Organic electroluminescent materials and devices

ABSTRACT

A novel compound is disclosed which includes a ligand LA of Formula II,wherein:ring B is independently a 5-membered or 6-membered carbocyclic or heterocyclic ring;X1 to X4 are each independently selected from the group consisting of C, N, and CR;at least one pair of adjacent X1 to X4 are each C and fused to Formula Vwhere indicated by “”; X5 to X12 are each independently C or N; the maximum number of N within a ring is two; Z and Y are each independently selected from the group consisting of O, S, Se, NR′, CR′R″, SiR′R″, and GeR′R″; RB and RC each independently represents zero, mono, or up to a maximum allowed substitutions to its associated ring; each of RB, RC, R, R′, and R″ is independently hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, boryl, and combinations thereof; and two substituents can be joined or fused to form a ring; the ligand LA is complexed to a metal M through the two indicated dash lines of each Formula; and the ligand LA can be joined with other ligands to form a tridentate, tetradentate, pentadentate, or hexadentate ligand.

CROSS-REFERENCE TO RELATED CASES

This application is a continuation of U.S. patent application Ser. No.16/828,080, filed Mar. 24, 2020, which (i) claims priority under U.S.C.§ 1.119(e) to U.S. Provisional application No. 62/930,837, filed on Nov.5, 2019, and (ii) is a continuation-in-part of U.S. patent applicationSer. No. 16/375,467, filed on Apr. 4, 2019, which is acontinuation-in-part of U.S. patent application Ser. No. 15/950,351,filed on Apr. 11, 2018, which is a continuation-in-part of U.S. patentapplication Ser. No. 15/825,297, filed on Nov. 29, 2017, which is acontinuation-in-part of co-pending U.S. patent application Ser. No.15/706,186, filed on Sep. 15, 2017, that claims priority to U.S.Provisional application No. 62/403,424, filed Oct. 3, 2016, thedisclosure of which is encorporated herein by reference.

FIELD

The present disclosure generally relates to organometallic compounds andformulations and their various uses including as emitters in devicessuch as organic light emitting diodes and related electronic devices.

BACKGROUND

Opto-electronic devices that make use of organic materials are becomingincreasingly desirable for a number of reasons. Many of the materialsused to make such devices are relatively inexpensive, so organicopto-electronic devices have the potential for cost advantages overinorganic devices. In addition, the inherent properties of organicmaterials, such as their flexibility, may make them well suited forparticular applications such as fabrication on a flexible substrate.Examples of organic opto-electronic devices include organic lightemitting diodes/devices (OLEDs), organic phototransistors, organicphotovoltaic cells, and organic photodetectors. For OLEDs, the organicmaterials may have performance advantages over conventional materials.For example, the wavelength at which an organic emissive layer emitslight may generally be readily tuned with appropriate dopants.

OLEDs make use of thin organic films that emit light when voltage isapplied across the device. OLEDs are becoming an increasinglyinteresting technology for use in applications such as flat paneldisplays, illumination, and backlighting. Several OLED materials andconfigurations are described in U.S. Pat. Nos. 5,844,363, 6,303,238, and5,707,745, which are incorporated herein by reference in their entirety.

One application for phosphorescent emissive molecules is a full colordisplay. Industry standards for such a display call for pixels adaptedto emit particular colors, referred to as “saturated” colors. Inparticular, these standards call for saturated red, green, and bluepixels. Alternatively the OLED can be designed to emit white light. Inconventional liquid crystal displays emission from a white backlight isfiltered using absorption filters to produce red, green and blueemission. The same technique can also be used with OLEDs. The white OLEDcan be either a single EML device or a stack structure. Color may bemeasured using CIE coordinates, which are well known to the art.

One example of a green emissive molecule is tris(2-phenylpyridine)iridium, denoted Ir(ppy)₃, which has the following structure:

In this, and later figures herein, we depict the dative bond fromnitrogen to metal (here, Ir) as a straight line.

As used herein, the term “organic” includes polymeric materials as wellas small molecule organic materials that may be used to fabricateorganic opto-electronic devices. “Small molecule” refers to any organicmaterial that is not a polymer, and “small molecules” may actually bequite large. Small molecules may include repeat units in somecircumstances. For example, using a long chain alkyl group as asubstituent does not remove a molecule from the “small molecule” class.Small molecules may also be incorporated into polymers, for example as apendent group on a polymer backbone or as a part of the backbone. Smallmolecules may also serve as the core moiety of a dendrimer, whichconsists of a series of chemical shells built on the core moiety. Thecore moiety of a dendrimer may be a fluorescent or phosphorescent smallmolecule emitter. A dendrimer may be a “small molecule,” and it isbelieved that all dendrimers currently used in the field of OLEDs aresmall molecules.

As used herein, “top” means furthest away from the substrate, while“bottom” means closest to the substrate. Where a first layer isdescribed as “disposed over” a second layer, the first layer is disposedfurther away from substrate. There may be other layers between the firstand second layer, unless it is specified that the first layer is “incontact with” the second layer. For example, a cathode may be describedas “disposed over” an anode, even though there are various organiclayers in between.

As used herein, “solution processable” means capable of being dissolved,dispersed, or transported in and/or deposited from a liquid medium,either in solution or suspension form.

A ligand may be referred to as “photoactive” when it is believed thatthe ligand directly contributes to the photoactive properties of anemissive material. A ligand may be referred to as “ancillary” when it isbelieved that the ligand does not contribute to the photoactiveproperties of an emissive material, although an ancillary ligand mayalter the properties of a photoactive ligand.

As used herein, and as would be generally understood by one skilled inthe art, a first “Highest Occupied Molecular Orbital” (HOMO) or “LowestUnoccupied Molecular Orbital” (LUMO) energy level is “greater than” or“higher than” a second HOMO or LUMO energy level if the first energylevel is closer to the vacuum energy level. Since ionization potentials(IP) are measured as a negative energy relative to a vacuum level, ahigher HOMO energy level corresponds to an IP having a smaller absolutevalue (an IP that is less negative). Similarly, a higher LUMO energylevel corresponds to an electron affinity (EA) having a smaller absolutevalue (an EA that is less negative). On a conventional energy leveldiagram, with the vacuum level at the top, the LUMO energy level of amaterial is higher than the HOMO energy level of the same material. A“higher” HOMO or LUMO energy level appears closer to the top of such adiagram than a “lower” HOMO or LUMO energy level.

As used herein, and as would be generally understood by one skilled inthe art, a first work function is “greater than” or “higher than” asecond work function if the first work function has a higher absolutevalue. Because work functions are generally measured as negative numbersrelative to vacuum level, this means that a “higher” work function ismore negative. On a conventional energy level diagram, with the vacuumlevel at the top, a “higher” work function is illustrated as furtheraway from the vacuum level in the downward direction. Thus, thedefinitions of HOMO and LUMO energy levels follow a different conventionthan work functions.

More details on OLEDs, and the definitions described above, can be foundin U.S. Pat. No. 7,279,704, which is incorporated herein by reference inits entirety.

SUMMARY

In one aspect, the present disclosure provides a compound comprising aligand L_(A) of Formula I, Formula II, Formula III, or Formula IV:

where: ring B is independently a 5-membered or 6-membered carbocyclic orheterocyclic ring; X¹ to X⁴ are each independently selected from thegroup consisting of C, N, and CR; at least one pair of adjacent X¹ to X⁴are each C and fused to a structure of Formula V

where indicated by “

”; “X⁵ to X¹² are each independently C or N; Z and Y are eachindependently selected from the group consisting of O, S, Se, NR′,CR′R”, SiR′R″, and GeR′R″; R^(B) and R^(C) each independently representszero, mono, or up to a maximum allowed substitutions to its associatedring; each of R^(B), R^(C), R, R′, and R″ is independently a hydrogen ora substituent selected from the group consisting of the generalsubstituents defined herein; and two substituents can be joined or fusedto form a ring; the ligand L_(A) is complexed to a metal M through thetwo indicated dash lines of each Formula I, Formula II, Formula III, andFormula IV; and the ligand L_(A) can be joined with other ligands toform a tridentate, tetradentate, pentadentate, or hexadentate ligand.

In another aspect, the present disclosure provides a formulation of acompound comprising a ligand L_(A) of Formula I, Formula II, FormulaIII, or Formula IV as described herein.

In yet another aspect, the present disclosure provides an OLED having anorganic layer comprising a compound comprising a ligand L_(A) of FormulaI, Formula II, Formula III, or Formula IV as described herein.

In yet another aspect, the present disclosure provides a consumerproduct comprising an OLED with an organic layer comprising a compoundcomprising a ligand L_(A) of Formula I, Formula II, Formula III, orFormula IV as described herein.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows an organic light emitting device.

FIG. 2 shows an inverted organic light emitting device that does nothave a separate electron transport layer.

FIG. 3 is a plot of photoluminescence (PL) spectra of the InventiveExample compound 1 and 2 and the Comparative Example compound 1 taken in2-methylTHF solution at room temperature.

DETAILED DESCRIPTION

Generally, an OLED comprises at least one organic layer disposed betweenand electrically connected to an anode and a cathode. When a current isapplied, the anode injects holes and the cathode injects electrons intothe organic layer(s). The injected holes and electrons each migratetoward the oppositely charged electrode. When an electron and holelocalize on the same molecule, an “exciton,” which is a localizedelectron-hole pair having an excited energy state, is formed. Light isemitted when the exciton relaxes via a photoemissive mechanism. In somecases, the exciton may be localized on an excimer or an exciplex.Non-radiative mechanisms, such as thermal relaxation, may also occur,but are generally considered undesirable.

The initial OLEDs used emissive molecules that emitted light from theirsinglet states (“fluorescence”) as disclosed, for example, in U.S. Pat.No. 4,769,292, which is incorporated by reference in its entirety.Fluorescent emission generally occurs in a time frame of less than 10nanoseconds.

More recently, OLEDs having emissive materials that emit light fromtriplet states (“phosphorescence”) have been demonstrated. Baldo et al.,“Highly Efficient Phosphorescent Emission from OrganicElectroluminescent Devices,” Nature, vol. 395, 151-154, 1998;(“Baldo-I”) and Baldo et al., “Very high-efficiency green organiclight-emitting devices based on electrophosphorescence,” Appl. Phys.Lett., vol. 75, No. 3, 4-6 (1999) (“Baldo-II”), are incorporated byreference in their entireties. Phosphorescence is described in moredetail in U.S. Pat. No. 7,279,704 at cols. 5-6, which are incorporatedby reference.

FIG. 1 shows an organic light emitting device 100. The figures are notnecessarily drawn to scale. Device 100 may include a substrate 110, ananode 115, a hole injection layer 120, a hole transport layer 125, anelectron blocking layer 130, an emissive layer 135, a hole blockinglayer 140, an electron transport layer 145, an electron injection layer150, a protective layer 155, a cathode 160, and a barrier layer 170.Cathode 160 is a compound cathode having a first conductive layer 162and a second conductive layer 164. Device 100 may be fabricated bydepositing the layers described, in order. The properties and functionsof these various layers, as well as example materials, are described inmore detail in U.S. Pat. No. 7,279,704 at cols. 6-10, which areincorporated by reference.

More examples for each of these layers are available. For example, aflexible and transparent substrate-anode combination is disclosed inU.S. Pat. No. 5,844,363, which is incorporated by reference in itsentirety. An example of a p-doped hole transport layer is m-MTDATA dopedwith F₄-TCNQ at a molar ratio of 50:1, as disclosed in U.S. PatentApplication Publication No. 2003/0230980, which is incorporated byreference in its entirety. Examples of emissive and host materials aredisclosed in U.S. Pat. No. 6,303,238 to Thompson et al., which isincorporated by reference in its entirety. An example of an n-dopedelectron transport layer is BPhen doped with Li at a molar ratio of 1:1,as disclosed in U.S. Patent Application Publication No. 2003/0230980,which is incorporated by reference in its entirety. U.S. Pat. Nos.5,703,436 and 5,707,745, which are incorporated by reference in theirentireties, disclose examples of cathodes including compound cathodeshaving a thin layer of metal such as Mg:Ag with an overlyingtransparent, electrically-conductive, sputter-deposited ITO layer. Thetheory and use of blocking layers is described in more detail in U.S.Pat. No. 6,097,147 and U.S. Patent Application Publication No.2003/0230980, which are incorporated by reference in their entireties.Examples of injection layers are provided in U.S. Patent ApplicationPublication No. 2004/0174116, which is incorporated by reference in itsentirety. A description of protective layers may be found in U.S. PatentApplication Publication No. 2004/0174116, which is incorporated byreference in its entirety.

FIG. 2 shows an inverted OLED 200. The device includes a substrate 210,a cathode 215, an emissive layer 220, a hole transport layer 225, and ananode 230. Device 200 may be fabricated by depositing the layersdescribed, in order. Because the most common OLED configuration has acathode disposed over the anode, and device 200 has cathode 215 disposedunder anode 230, device 200 may be referred to as an “inverted” OLED.Materials similar to those described with respect to device 100 may beused in the corresponding layers of device 200. FIG. 2 provides oneexample of how some layers may be omitted from the structure of device100.

The simple layered structure illustrated in FIGS. 1 and 2 is provided byway of non-limiting example, and it is understood that embodiments ofthe invention may be used in connection with a wide variety of otherstructures. The specific materials and structures described areexemplary in nature, and other materials and structures may be used.Functional OLEDs may be achieved by combining the various layersdescribed in different ways, or layers may be omitted entirely, based ondesign, performance, and cost factors. Other layers not specificallydescribed may also be included. Materials other than those specificallydescribed may be used. Although many of the examples provided hereindescribe various layers as comprising a single material, it isunderstood that combinations of materials, such as a mixture of host anddopant, or more generally a mixture, may be used. Also, the layers mayhave various sublayers. The names given to the various layers herein arenot intended to be strictly limiting. For example, in device 200, holetransport layer 225 transports holes and injects holes into emissivelayer 220, and may be described as a hole transport layer or a holeinjection layer. In one embodiment, an OLED may be described as havingan “organic layer” disposed between a cathode and an anode. This organiclayer may comprise a single layer, or may further comprise multiplelayers of different organic materials as described, for example, withrespect to FIGS. 1 and 2 .

Structures and materials not specifically described may also be used,such as OLEDs comprised of polymeric materials (PLEDs) such as disclosedin U.S. Pat. No. 5,247,190 to Friend et al., which is incorporated byreference in its entirety. By way of further example, OLEDs having asingle organic layer may be used. OLEDs may be stacked, for example asdescribed in U.S. Pat. No. 5,707,745 to Forrest et al, which isincorporated by reference in its entirety. The OLED structure maydeviate from the simple layered structure illustrated in FIGS. 1 and 2 .For example, the substrate may include an angled reflective surface toimprove out-coupling, such as a mesa structure as described in U.S. Pat.No. 6,091,195 to Forrest et al., and/or a pit structure as described inU.S. Pat. No. 5,834,893 to Bulovic et al., which are incorporated byreference in their entireties.

Unless otherwise specified, any of the layers of the various embodimentsmay be deposited by any suitable method. For the organic layers,preferred methods include thermal evaporation, ink-jet, such asdescribed in U.S. Pat. Nos. 6,013,982 and 6,087,196, which areincorporated by reference in their entireties, organic vapor phasedeposition (OVPD), such as described in U.S. Pat. No. 6,337,102 toForrest et al., which is incorporated by reference in its entirety, anddeposition by organic vapor jet printing (OVJP), such as described inU.S. Pat. No. 7,431,968, which is incorporated by reference in itsentirety. Other suitable deposition methods include spin coating andother solution based processes. Solution based processes are preferablycarried out in nitrogen or an inert atmosphere. For the other layers,preferred methods include thermal evaporation. Preferred patterningmethods include deposition through a mask, cold welding such asdescribed in U.S. Pat. Nos. 6,294,398 and 6,468,819, which areincorporated by reference in their entireties, and patterning associatedwith some of the deposition methods such as ink jet and organic vaporjet printing (OVJP). Other methods may also be used. The materials to bedeposited may be modified to make them compatible with a particulardeposition method. For example, substituents such as alkyl and arylgroups, branched or unbranched, and preferably containing at least 3carbons, may be used in small molecules to enhance their ability toundergo solution processing. Substituents having 20 carbons or more maybe used, and 3-20 carbons is a preferred range. Materials withasymmetric structures may have better solution processability than thosehaving symmetric structures, because asymmetric materials may have alower tendency to recrystallize. Dendrimer substituents may be used toenhance the ability of small molecules to undergo solution processing.

Devices fabricated in accordance with embodiments of the presentinvention may further optionally comprise a barrier layer. One purposeof the barrier layer is to protect the electrodes and organic layersfrom damaging exposure to harmful species in the environment includingmoisture, vapor and/or gases, etc. The barrier layer may be depositedover, under or next to a substrate, an electrode, or over any otherparts of a device including an edge. The barrier layer may comprise asingle layer, or multiple layers. The barrier layer may be formed byvarious known chemical vapor deposition techniques and may includecompositions having a single phase as well as compositions havingmultiple phases. Any suitable material or combination of materials maybe used for the barrier layer. The barrier layer may incorporate aninorganic or an organic compound or both. The preferred barrier layercomprises a mixture of a polymeric material and a non-polymeric materialas described in U.S. Pat. No. 7,968,146, PCT Pat. Application Nos.PCT/US2007/023098 and PCT/US2009/042829, which are herein incorporatedby reference in their entireties. To be considered a “mixture”, theaforesaid polymeric and non-polymeric materials comprising the barrierlayer should be deposited under the same reaction conditions and/or atthe same time. The weight ratio of polymeric to non-polymeric materialmay be in the range of 95:5 to 5:95. The polymeric material and thenon-polymeric material may be created from the same precursor material.In one example, the mixture of a polymeric material and a non-polymericmaterial consists essentially of polymeric silicon and inorganicsilicon.

Devices fabricated in accordance with embodiments of the invention canbe incorporated into a wide variety of electronic component modules (orunits) that can be incorporated into a variety of electronic products orintermediate components. Examples of such electronic products orintermediate components include display screens, lighting devices suchas discrete light source devices or lighting panels, etc. that can beutilized by the end-user product manufacturers. Such electroniccomponent modules can optionally include the driving electronics and/orpower source(s). Devices fabricated in accordance with embodiments ofthe invention can be incorporated into a wide variety of consumerproducts that have one or more of the electronic component modules (orunits) incorporated therein. A consumer product comprising an OLED thatincludes the compound of the present disclosure in the organic layer inthe OLED is disclosed. Such consumer products would include any kind ofproducts that include one or more light source(s) and/or one or more ofsome type of visual displays. Some examples of such consumer productsinclude flat panel displays, curved displays, computer monitors, medicalmonitors, televisions, billboards, lights for interior or exteriorillumination and/or signaling, heads-up displays, fully or partiallytransparent displays, flexible displays, rollable displays, foldabledisplays, stretchable displays, laser printers, telephones, mobilephones, tablets, phablets, personal digital assistants (PDAs), wearabledevices, laptop computers, digital cameras, camcorders, viewfinders,micro-displays (displays that are less than 2 inches diagonal), 3-Ddisplays, virtual reality or augmented reality displays, vehicles, videowalls comprising multiple displays tiled together, theater or stadiumscreen, a light therapy device, and a sign. Various control mechanismsmay be used to control devices fabricated in accordance with the presentinvention, including passive matrix and active matrix. Many of thedevices are intended for use in a temperature range comfortable tohumans, such as 18 degrees C. to 30 degrees C., and more preferably atroom temperature (20-25 degrees C.), but could be used outside thistemperature range, for example, from −40 degree C. to +80 degree C.

The materials and structures described herein may have applications indevices other than OLEDs. For example, other optoelectronic devices suchas organic solar cells and organic photodetectors may employ thematerials and structures. More generally, organic devices, such asorganic transistors, may employ the materials and structures.

The terms “halo,” “halogen,” and “halide” are used interchangeably andrefer to fluorine, chlorine, bromine, and iodine.

The term “acyl” refers to a substituted carbonyl radical (C(O)—R_(S)).

The term “ester” refers to a substituted oxycarbonyl (—O—C(O)—R_(S) or—C(O)—O—R_(S)) radical.

The term “ether” refers to an —OR_(S) radical.

The terms “sulfanyl” or “thio-ether” are used interchangeably and referto a —SR_(S) radical.

The term “sulfinyl” refers to a —S(O)—R_(S) radical.

The term “sulfonyl” refers to a —SO₂—R_(S) radical.

The term “phosphino” refers to a —P(R_(S))₃ radical, wherein each R_(S)can be same or different.

The term “silyl” refers to a —Si(R_(S))₃ radical, wherein each R_(S) canbe same or different.

The term “boryl” refers to a —B(R_(s))₂ radical or its Lewis adduct—B(R_(s))₃ radical, wherein R_(s) can be same or different.

In each of the above, R_(S) can be hydrogen or a substituent selectedfrom the group consisting of deuterium, halogen, alkyl, cycloalkyl,heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl,alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, andcombination thereof. Preferred R_(s) is selected from the groupconsisting of alkyl, cycloalkyl, aryl, heteroaryl, and combinationthereof.

The term “alkyl” refers to and includes both straight and branched chainalkyl radicals. Preferred alkyl groups are those containing from one tofifteen carbon atoms and includes methyl, ethyl, propyl, 1-methylethyl,butyl, 1-methylpropyl, 2-methylpropyl, pentyl, 1-methylbutyl,2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl,2,2-dimethylpropyl, and the like. Additionally, the alkyl group isoptionally substituted.

The term “cycloalkyl” refers to and includes monocyclic, polycyclic, andspiro alkyl radicals. Preferred cycloalkyl groups are those containing 3to 12 ring carbon atoms and includes cyclopropyl, cyclopentyl,cyclohexyl, bicyclo[3.1.1]heptyl, spiro[4.5]decyl, spiro[5.5]undecyl,adamantyl, and the like. Additionally, the cycloalkyl group isoptionally substituted.

The terms “heteroalkyl” or “heterocycloalkyl” refer to an alkyl or acycloalkyl radical, respectively, having at least one carbon atomreplaced by a heteroatom. Optionally the at least one heteroatom isselected from O, S, N, P, B, Si and Se, preferably, O, S or N.Additionally, the heteroalkyl or heterocycloalkyl group is optionallysubstituted.

The term “alkenyl” refers to and includes both straight and branchedchain alkene radicals. Alkenyl groups are essentially alkyl groups thatinclude at least one carbon-carbon double bond in the alkyl chain.Cycloalkenyl groups are essentially cycloalkyl groups that include atleast one carbon-carbon double bond in the cycloalkyl ring. The term“heteroalkenyl” as used herein refers to an alkenyl radical having atleast one carbon atom replaced by a heteroatom. Optionally the at leastone heteroatom is selected from O, S, N, P, B, Si, and Se, preferably,O, S, or N. Preferred alkenyl, cycloalkenyl, or heteroalkenyl groups arethose containing two to fifteen carbon atoms. Additionally, the alkenyl,cycloalkenyl, or heteroalkenyl group is optionally substituted.

The term “alkynyl” refers to and includes both straight and branchedchain alkyne radicals. Preferred alkynyl groups are those containing twoto fifteen carbon atoms. Additionally, the alkynyl group is optionallysubstituted.

The terms “aralkyl” or “arylalkyl” are used interchangeably and refer toan alkyl group that is substituted with an aryl group. Additionally, thearalkyl group is optionally substituted.

The term “heterocyclic group” refers to and includes aromatic andnon-aromatic cyclic radicals containing at least one heteroatom.Optionally the at least one heteroatom is selected from O, S, N, P, B,Si, and Se, preferably, O, S, or N. Hetero-aromatic cyclic radicals maybe used interchangeably with heteroaryl. Preferred hetero-non-aromaticcyclic groups are those containing 3 to 7 ring atoms which includes atleast one hetero atom, and includes cyclic amines such as morpholino,piperidino, pyrrolidino, and the like, and cyclic ethers/thio-ethers,such as tetrahydrofuran, tetrahydropyran, tetrahydrothiophene, and thelike. Additionally, the heterocyclic group may be optionallysubstituted.

The term “aryl” refers to and includes both single-ring aromatichydrocarbyl groups and polycyclic aromatic ring systems. The polycyclicrings may have two or more rings in which two carbons are common to twoadjoining rings (the rings are “fused”) wherein at least one of therings is an aromatic hydrocarbyl group, e.g., the other rings can becycloalkyls, cycloalkenyls, aryl, heterocycles, and/or heteroaryls.Preferred aryl groups are those containing six to thirty carbon atoms,preferably six to twenty carbon atoms, more preferably six to twelvecarbon atoms. Especially preferred is an aryl group having six carbons,ten carbons or twelve carbons. Suitable aryl groups include phenyl,biphenyl, triphenyl, triphenylene, tetraphenylene, naphthalene,anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene,perylene, and azulene, preferably phenyl, biphenyl, triphenyl,triphenylene, fluorene, and naphthalene. Additionally, the aryl group isoptionally substituted.

The term “heteroaryl” refers to and includes both single-ring aromaticgroups and polycyclic aromatic ring systems that include at least oneheteroatom. The heteroatoms include, but are not limited to O, S, N, P,B, Si, and Se. In many instances, O, S, or N are the preferredheteroatoms. Hetero-single ring aromatic systems are preferably singlerings with 5 or 6 ring atoms, and the ring can have from one to sixheteroatoms. The hetero-polycyclic ring systems can have two or morerings in which two atoms are common to two adjoining rings (the ringsare “fused”) wherein at least one of the rings is a heteroaryl, e.g.,the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles,and/or heteroaryls. The hetero-polycyclic aromatic ring systems can havefrom one to six heteroatoms per ring of the polycyclic aromatic ringsystem. Preferred heteroaryl groups are those containing three to thirtycarbon atoms, preferably three to twenty carbon atoms, more preferablythree to twelve carbon atoms. Suitable heteroaryl groups includedibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene,benzofuran, benzothiophene, benzoselenophene, carbazole,indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole,triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole,thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine,oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole,indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline,isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine,phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine,phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine,thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine,preferably dibenzothiophene, dibenzofuran, dibenzoselenophene,carbazole, indolocarbazole, imidazole, pyridine, triazine,benzimidazole, 1,2-azaborine, 1,3-azaborine, 1,4-azaborine, borazine,and aza-analogs thereof. Additionally, the heteroaryl group isoptionally substituted.

Of the aryl and heteroaryl groups listed above, the groups oftriphenylene, naphthalene, anthracene, dibenzothiophene, dibenzofuran,dibenzoselenophene, carbazole, indolocarbazole, imidazole, pyridine,pyrazine, pyrimidine, triazine, and benzimidazole, and the respectiveaza-analogs of each thereof are of particular interest.

The terms alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, alkenyl,cycloalkenyl, heteroalkenyl, alkynyl, aralkyl, heterocyclic group, aryl,and heteroaryl, as used herein, are independently unsubstituted, orindependently substituted, with one or more general substituents.

In many instances, the general substituents are selected from the groupconsisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl,heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl,cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylicacid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl,phosphino, boryl, and combinations thereof.

In some instances, the preferred general substituents are selected fromthe group consisting of deuterium, fluorine, alkyl, cycloalkyl,heteroalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl,heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, sulfanyl, boryl,and combinations thereof.

In some instances, the more preferred general substituents are selectedfrom the group consisting of deuterium, fluorine, alkyl, cycloalkyl,alkoxy, aryloxy, amino, silyl, aryl, heteroaryl, sulfanyl, andcombinations thereof.

In yet other instances, the most preferred general substituents areselected from the group consisting of deuterium, fluorine, alkyl,cycloalkyl, aryl, heteroaryl, and combinations thereof.

The terms “substituted” and “substitution” refer to a substituent otherthan H that is bonded to the relevant position, e.g., a carbon ornitrogen. For example, when R¹ represents mono-substitution, then one R¹must be other than H (i.e., a substitution). Similarly, when R¹represents di-substitution, then two of R¹ must be other than H.Similarly, when R¹ represents no substitution, R¹, for example, can be ahydrogen for available valencies of ring atoms, as in carbon atoms forbenzene and the nitrogen atom in pyrrole, or simply represents nothingfor ring atoms with fully filled valencies, e.g., the nitrogen atom inpyridine. The maximum number of substitutions possible in a ringstructure will depend on the total number of available valencies in thering atoms.

As used herein, “combinations thereof” indicates that one or moremembers of the applicable list are combined to form a known orchemically stable arrangement that one of ordinary skill in the art canenvision from the applicable list. For example, an alkyl and deuteriumcan be combined to form a partial or fully deuterated alkyl group; ahalogen and alkyl can be combined to form a halogenated alkylsubstituent; and a halogen, alkyl, and aryl can be combined to form ahalogenated arylalkyl. In one instance, the term substitution includes acombination of two to four of the listed groups. In another instance,the term substitution includes a combination of two to three groups. Inyet another instance, the term substitution includes a combination oftwo groups. Preferred combinations of substituent groups are those thatcontain up to fifty atoms that are not hydrogen or deuterium, or thosewhich include up to forty atoms that are not hydrogen or deuterium, orthose that include up to thirty atoms that are not hydrogen ordeuterium. In many instances, a preferred combination of substituentgroups will include up to twenty atoms that are not hydrogen ordeuterium.

The “aza” designation in the fragments described herein, i.e.aza-dibenzofuran, aza-dibenzothiophene, etc. means that one or more ofthe C—H groups in the respective aromatic ring can be replaced by anitrogen atom, for example, and without any limitation, azatriphenyleneencompasses both dibenzo[f,h]quinoxaline and dibenzo[f,h]quinoline. Oneof ordinary skill in the art can readily envision other nitrogen analogsof the aza-derivatives described above, and all such analogs areintended to be encompassed by the terms as set forth herein.

As used herein, “deuterium” refers to an isotope of hydrogen. Deuteratedcompounds can be readily prepared using methods known in the art. Forexample, U.S. Pat. No. 8,557,400, Patent Pub. No. WO 2006/095951, andU.S. Pat. Application Pub. No. US 2011/0037057, which are herebyincorporated by reference in their entireties, describe the making ofdeuterium-substituted organometallic complexes. Further reference ismade to Ming Yan, et al., Tetrahedron 2015, 71, 1425-30 and Atzrodt etal., Angew. Chem. Int. Ed. (Reviews) 2007, 46, 7744-65, which areincorporated by reference in their entireties, describe the deuterationof the methylene hydrogens in benzyl amines and efficient pathways toreplace aromatic ring hydrogens with deuterium, respectively.

It is to be understood that when a molecular fragment is described asbeing a substituent or otherwise attached to another moiety, its namemay be written as if it were a fragment (e.g. phenyl, phenylene,naphthyl, dibenzofuryl) or as if it were the whole molecule (e.g.benzene, naphthalene, dibenzofuran). As used herein, these differentways of designating a substituent or attached fragment are considered tobe equivalent.

In some instance, a pair of adjacent substituents can be optionallyjoined or fused into a ring. The preferred ring is a five, six, orseven-membered carbocyclic or heterocyclic ring, includes both instanceswhere the portion of the ring formed by the pair of substituents issaturated and where the portion of the ring formed by the pair ofsubstituents is unsaturated. As used herein, “adjacent” means that thetwo substituents involved can be on the same ring next to each other, oron two neighboring rings having the two closest available substitutablepositions, such as 2, 2′ positions in a biphenyl, or 1, 8 position in anaphthalene, as long as they can form a stable fused ring system.

The Compounds of the Present Disclosure

In one aspect, the present disclosure provides a compound comprising aligand L_(A) of Formula I, Formula II, Formula III, or Formula IV:

where: ring B is independently a 5-membered or 6-membered carbocyclic orheterocyclic ring; X¹ to X⁴ are each independently selected from thegroup consisting of C, N, and CR; at least one pair of adjacent X¹ to X⁴are each C and fused to a structure of Formula V

where indicated by “

”; X⁵ to X¹² are each independently C or N; Z and Y are eachindependently selected from the group consisting of O, S, Se, NR′,CR′R″, SiR′R″, and GeR′R″; R^(B) and R^(C) each independently representszero, mono, or up to a maximum allowed substitutions to its associatedring; each of R^(B), R^(C), R, R′, and R″ is independently a hydrogen ora substituent selected from the group consisting of the generalsubstituents defined herein; and two substituents can be joined or fusedto form a ring; the ligand L_(A) is complexed to a metal M through thetwo indicated dash lines of each Formula I, Formula II, Formula III, andFormula IV; and the ligand L_(A) can be joined with other ligands toform a tridentate, tetradentate, pentadentate, or hexadentate ligand.

In some embodiments of the compound, the maximum number of N within aring in the ligand L_(A) is two.

In some embodiments of the compound, each of R^(B), R^(C), R, R′, and R″is independently a hydrogen or a substituent selected from the groupconsisting of the preferred general substituents defined herein.

In some embodiments of the compound, ring B is a 6-membered ring. Insome embodiments where ring B is a 6-membered ring, each R is H.

In some embodiments of the compound, the ligand L_(A) is selected fromthe group consisting of the following structures:

wherein the relevant provisos for Formulas I and II apply to Formulas VIand VII.

In any of the embodiments of the compound mentioned above, each of X¹ toX⁴ is independently C or CR.

In some embodiments of the compound, at least one of X¹ to X⁴ in eachformula is N.

In some embodiments of the compound, each of X⁵ to X⁸ is C.

In some embodiments of the compound, each of X⁹ to X¹² is C.

In some embodiments of the compound, each of X⁵ to X¹² is C.

In some embodiments of the compound, at least one of X⁵ to X¹² in eachformula is N.

In some embodiments of the compound, at least one of X⁵ to X⁸ in eachformula is N.

In some embodiments of the compound, at least one of X⁹ to X¹² in eachformula is N.

In some embodiments of the compound, Z for each occurrence independentlyforms a direct bond to X¹. In some embodiments, Z for each occurrenceindependently forms a direct bond to X². In some embodiments, Z for eachoccurrence independently forms a direct bond to X³. In some embodiments,Z for each occurrence independently forms a direct bond to X⁴. In someembodiments, Z for each occurrence is independently O or S.

In some embodiments of the compound, each R^(C) in each of the FormulasI, II, III, and IV is H. In some embodiments, at least one R^(B) in eachof the Formulas I, II, III, IV, VI, and VII is independently an alkyl orcycloalkyl group. In some embodiments, at least one R^(B) in each of theFormulas I, II, III, and IV is independently a tertiary alkyl group.

In some embodiments of the compound, Y for each occurrence isindependently O or S.

In some embodiments of the compound, the ligand L_(A) is selected fromthe Ligand Group A consisting of the following structures:

In some embodiments of the compound, the compound comprises the ligandL_(A) selected from the Ligand Group B consisting of the followingstructures:

In some embodiments of the compound where the ligand L_(A) is selectedfrom the Ligand Group A or the Ligand Group B, each of R^(B), R^(C), R,R′, and R″ for each Formula is independently hydrogen or a substituentselected from the group consisting of the preferred general substituentsdefined herein.

In some embodiments of the compound where the ligand L_(A) is selectedfrom the Ligand Group B, the R^(B) substituent is para to the metal andis selected from the group consisting of alkyl, cycloalkyl, andcombination thereof.

In some embodiments of the compound where the ligand L_(A) is selectedfrom the Ligand Group B, the R^(B) substituent is para to the metal andis a tertiary alkyl. In some embodiments, the R^(B) substituent is parato the metal and is tert-butyl.

In some embodiments of the compound where the ligand L_(A) is selectedfrom the Ligand Group A, X¹ to X⁴ for each formula in Ligand Group A areindependently C or CR. In some embodiments, each R for each formula inLigand Group A is independently H. In some embodiments, each of X⁵ to X⁸for each formula in Ligand Group A is independently C. In someembodiments, each of X⁹ to X¹² for each formula in Ligand Group A isindependently C. In some embodiments, each of X⁵ to X¹² for each formulain Ligand Group A is independently C. In some embodiments, at least oneof X⁵ to X¹² for each formula in Ligand Group A is independently N. Insome embodiments, at least one of X⁵ to X⁸ for each formula in LigandGroup A is independently N. In some embodiments, at least one of X⁹ toX¹² for each formula in Ligand Group A is independently N. In someembodiments, each R^(C) for each formula in Ligand Group A isindependently H. In some embodiments, at least one R^(B) for eachformula in Ligand Group A is independently an alkyl, cycloalkyl, orcombination thereof. In some embodiments, at least one R^(B) for eachformula in Ligand Group A is independently a tertiary alkyl group. Insome embodiments, Z for each occurrence is independently O or S.

In some embodiments of the compound, the compound comprises asubstituted or unsubstituted acetylacetonate ligand. In some embodimentsof the compound, the metal M is selected from the group consisting ofOs, Ir, Pd, Pt, Cu, Ag, and Au. In some embodiments of the compound, themetal M is selected from the group consisting of Ir and Pt. In someembodiments of the compound, the compound comprises the ligand L_(A)selected from the group consisting of:

where each of R^(B) can be the same or different, each of R^(C) can bethe same or different, and R^(B) and R^(C) for each occurrence isindependently selected from the group consisting of the generalsubstituents defined herein.

In some embodiments of the compound, the compound comprises the ligandL_(A) selected from the group consisting of

L_(Ai-1) based on Structure 1:

L_(Ai-2) based on Structure 2:

L_(Ai-3) based on Structure 3:

L_(Ai-4) based on Structure 4:

L_(Ai-5) based on Structure 5:

L_(Ai-6) based on Structure 6:

L_(Ai-7) based on Structure 7:

L_(Ai-8) based on Structure 8:

L_(Ai-9) based on Structure 9:

L_(Ai-10) based on Structure 10:

L_(Ai-11) based on Structure 11:

L_(Ai-12) based on Structure 12:

L_(Ai-13) based on Structure 13:

L_(Ai-14) based on Structure 14:

L_(Ai-15) based on Structure 15:

L_(Ai-16) based on Structure 16:

L_(Ai-17) based on Structure 17:

L_(Ai-18) based on Structure 18:

L_(Ai-19) based on Structure 19:

L_(Ai-20) based on Structure 20:

L_(Ai-21) based on Structure 21:

L_(Ai-22) based on Structure 22:

L_(Ai-23) based on Structure 23:

L_(Ai-24) based on Structure 24:

L_(Ai-25) based on Structure 25:

L_(Ai-26) based on Structure 26:

L_(Ai-27) based on Structure 27:

L_(Ai-28) based on Structure 28:

L_(Ai-29) based on Structure 29:

L_(Ai-30) based on Structure 30:

L_(Ai-31) based on Structure 31:

L_(Ai-32) based on Structure 32:

L_(Ai-33) based on Structure 33:

L_(Ai-34) based on Structure 34:

L_(Ai-35) based on Structure 35:

wherein i is an integer from 1 to 1336, and for each i, R_(E), R_(F),and G are defined as below:

i R_(E) R_(F) G 1 R¹ R¹ G⁵ 2 R² R² G⁵ 3 R³ R³ G⁵ 4 R⁴ R⁴ G⁵ 5 R⁵ R⁵ G⁵ 6R⁶ R⁶ G⁵ 7 R⁷ R⁷ G⁵ 8 R⁸ R⁸ G⁵ 9 R⁹ R⁹ G⁵ 10 R¹⁰ R¹⁰ G⁵ 11 R¹¹ R¹¹ G⁵ 12R¹² R¹² G⁵ 13 R¹³ R¹³ G⁵ 14 R¹⁴ R¹⁴ G⁵ 15 R¹⁵ R¹⁵ G⁵ 16 R¹⁶ R¹⁶ G⁵ 17R¹⁷ R¹⁷ G⁵ 18 R¹⁸ R¹⁸ G⁵ 19 R¹⁹ R¹⁹ G⁵ 20 R²⁰ R²⁰ G⁵ 21 R²¹ R²¹ G⁵ 22R²² R²² G⁵ 23 R²³ R²³ G⁵ 24 R²⁴ R²⁴ G⁵ 25 R²⁵ R²⁵ G⁵ 26 R²⁶ R²⁶ G⁵ 27R²⁷ R²⁷ G⁵ 28 R²⁸ R²⁸ G⁵ 29 R²⁹ R²⁹ G⁵ 30 R³⁰ R³⁰ G⁵ 31 R³¹ R³¹ G⁵ 32R³² R³² G⁵ 31 R² R¹ G⁵ 32 R³ R¹ G⁵ 33 R⁴ R¹ G⁵ 34 R⁵ R¹ G⁵ 35 R⁶ R¹ G⁵36 R⁷ R¹ G⁵ 37 R⁸ R¹ G⁵ 38 R⁹ R¹ G⁵ 39 R¹⁰ R¹ G⁵ 40 R¹¹ R¹ G⁵ 41 R¹² R¹G⁵ 42 R¹³ R¹ G⁵ 43 R¹⁴ R¹ G⁵ 44 R¹⁵ R¹ G⁵ 45 R¹⁶ R¹ G⁵ 46 R¹⁷ R¹ G⁵ 47R¹⁸ R¹ G⁵ 48 R¹⁹ R¹ G⁵ 49 R²⁰ R¹ G⁵ 50 R²¹ R¹ G⁵ 51 R²² R¹ G⁵ 52 R²³ R¹G⁵ 53 R²⁴ R¹ G⁵ 54 R²⁵ R¹ G⁵ 55 R²⁶ R¹ G⁵ 56 R²⁷ R¹ G⁵ 57 R²⁸ R¹ G⁵ 58R²⁹ R¹ G⁵ 59 R³⁰ R¹ G⁵ 60 R³¹ R¹ G⁵ 61 R³² R¹ G⁵ 62 R¹ R² G⁵ 63 R¹ R³ G⁵64 R¹ R⁴ G⁵ 65 R¹ R⁵ G⁵ 66 R¹ R⁶ G⁵ 67 R¹ R⁷ G⁵ 68 R¹ R⁸ G⁵ 69 R¹ R⁹ G⁵70 R¹ R¹⁰ G⁵ 71 R¹ R¹¹ G⁵ 72 R¹ R¹² G⁵ 73 R¹ R¹³ G⁵ 74 R¹ R¹⁴ G⁵ 75 R¹R¹⁵ G⁵ 76 R¹ R¹⁶ G⁵ 77 R¹ R¹⁷ G⁵ 78 R¹ R¹⁸ G⁵ 79 R¹ R¹⁹ G⁵ 80 R¹ R²⁰ G⁵81 R¹ R²¹ G⁵ 82 R¹ R²² G⁵ 83 R¹ R²³ G⁵ 84 R¹ R²⁴ G⁵ 85 R¹ R²⁵ G⁵ 86 R¹R²⁶ G⁵ 87 R¹ R²⁷ G⁵ 88 R¹ R²⁸ G⁵ 89 R¹ R²⁹ G⁵ 90 R¹ R³⁰ G⁵ 91 R¹ R³¹ G⁵92 R¹ R³² G⁵ 93 R³ R² G⁵ 94 R⁴ R² G⁵ 95 R⁵ R² G⁵ 96 R⁶ R² G⁵ 97 R⁷ R² G⁵98 R⁸ R² G⁵ 99 R⁹ R² G⁵ 100 R¹⁰ R² G⁵ 101 R¹¹ R² G⁵ 102 R¹² R² G⁵ 103R¹³ R² G⁵ 104 R¹⁴ R² G⁵ 105 R¹⁵ R² G⁵ 106 R¹⁶ R² G⁵ 107 R¹⁷ R² G⁵ 108R¹⁸ R² G⁵ 109 R¹⁹ R² G⁵ 110 R²⁰ R² G⁵ 111 R²¹ R² G⁵ 112 R²² R² G⁵ 113R²³ R² G⁵ 114 R²⁴ R² G⁵ 115 R²⁵ R² G⁵ 116 R²⁶ R² G⁵ 117 R²⁷ R² G⁵ 118R²⁸ R² G⁵ 119 R²⁹ R² G⁵ 120 R³⁰ R² G⁵ 121 R³¹ R² G⁵ 122 R³² R² G⁵ 123 R²R³ G⁵ 124 R² R⁴ G⁵ 125 R² R⁵ G⁵ 126 R² R⁶ G⁵ 127 R² R⁷ G⁵ 128 R² R⁸ G⁵129 R² R⁹ G⁵ 130 R² R¹⁰ G⁵ 131 R² R¹¹ G⁵ 132 R² R¹² G⁵ 133 R² R¹³ G⁵ 134R² R¹⁴ G⁵ 135 R² R¹⁵ G⁵ 136 R² R¹⁶ G⁵ 137 R² R¹⁷ G⁵ 138 R² R¹⁸ G⁵ 139 R²R¹⁹ G⁵ 140 R² R²⁰ G⁵ 141 R² R²¹ G⁵ 142 R² R²² G⁵ 143 R² R²³ G⁵ 144 R²R²⁴ G⁵ 145 R² R²⁵ G⁵ 146 R² R²⁶ G⁵ 147 R² R²⁷ G⁵ 148 R² R²⁸ G⁵ 149 R²R²⁹ G⁵ 150 R² R³⁰ G⁵ 151 R² R³¹ G⁵ 152 R² R³² G⁵ 153 R² R³² G⁵ 154 R³R³² G⁵ 155 R⁴ R³² G⁵ 156 R⁵ R³² G⁵ 157 R⁶ R³² G⁵ 158 R⁷ R³² G⁵ 159 R⁸R³² G⁵ 160 R⁹ R³² G⁵ 161 R¹⁰ R³² G⁵ 162 R¹¹ R³² G⁵ 163 R¹² R³² G⁵ 164R¹³ R³² G⁵ 165 R¹⁴ R³² G⁵ 166 R¹⁵ R³² G⁵ 167 R¹⁶ R³² G⁵ 168 R¹⁷ R³² G⁵169 R¹⁸ R³² G⁵ 170 R¹⁹ R³² G⁵ 171 R²⁰ R³² G⁵ 172 R²¹ R³² G⁵ 173 R²² R³²G⁵ 174 R²³ R³² G⁵ 175 R²⁴ R³² G⁵ 176 R²⁵ R³² G⁵ 177 R²⁶ R³² G⁵ 178 R²⁷R³² G⁵ 179 R²⁸ R³² G⁵ 180 R²⁹ R³² G⁵ 181 R³⁰ R³² G⁵ 182 R³¹ R³² G⁵ 183R³² R² G⁵ 184 R³² R³ G⁵ 185 R³² R⁴ G⁵ 186 R³² R⁵ G⁵ 187 R³² R⁶ G⁵ 188R³² R⁷ G⁵ 189 R³² R⁸ G⁵ 190 R³² R⁹ G⁵ 191 R³² R¹⁰ G⁵ 192 R³² R¹¹ G⁵ 193R³² R¹² G⁵ 194 R³² R¹³ G⁵ 195 R³² R¹⁴ G⁵ 196 R³² R¹⁵ G⁵ 197 R³² R¹⁶ G⁵198 R³² R¹⁷ G⁵ 199 R³² R¹⁸ G⁵ 200 R³² R¹⁹ G⁵ 201 R³² R²⁰ G⁵ 202 R³² R²¹G⁵ 203 R³² R²² G⁵ 204 R³² R²³ G⁵ 205 R³² R²⁴ G⁵ 206 R³² R²⁵ G⁵ 207 R³²R²⁶ G⁵ 208 R³² R²⁷ G⁵ 209 R³² R²⁸ G⁵ 210 R³² R²⁹ G⁵ 211 R³² R³⁰ G⁵ 212R³² R³¹ G⁵ 213 R¹ R¹ G⁶ 214 R² R² G⁶ 215 R³ R³ G⁶ 216 R⁴ R⁴ G⁶ 217 R⁵ R⁵G⁶ 218 R⁶ R⁶ G⁶ 219 R⁷ R⁷ G⁶ 220 R⁸ R⁸ G⁶ 221 R⁹ R⁹ G⁶ 222 R¹⁰ R¹⁰ G⁶223 R¹¹ R¹¹ G⁶ 224 R¹² R¹² G⁶ 225 R¹³ R¹³ G⁶ 226 R¹⁴ R¹⁴ G⁶ 227 R¹⁵ R¹⁵G⁶ 228 R¹⁶ R¹⁶ G⁶ 229 R¹⁷ R¹⁷ G⁶ 230 R¹⁸ R¹⁸ G⁶ 231 R¹⁹ R¹⁹ G⁶ 232 R²⁰R²⁰ G⁶ 233 R²¹ R²¹ G⁶ 234 R²² R²² G⁶ 235 R²³ R²³ G⁶ 236 R²⁴ R²⁴ G⁶ 237R²⁵ R²⁵ G⁶ 238 R²⁶ R²⁶ G⁶ 239 R²⁷ R²⁷ G⁶ 240 R²⁸ R²⁸ G⁶ 241 R²⁹ R²⁹ G⁶242 R³⁰ R³⁰ G⁶ 243 R³¹ R³¹ G⁶ 244 R³² R³² G⁶ 245 R² R¹ G⁶ 246 R³ R¹ G⁶247 R⁴ R¹ G⁶ 248 R⁵ R¹ G⁶ 249 R⁶ R¹ G⁶ 250 R⁷ R¹ G⁶ 251 R⁸ R¹ G⁶ 252 R⁹R¹ G⁶ 253 R¹⁰ R¹ G⁶ 254 R¹¹ R¹ G⁶ 255 R¹² R¹ G⁶ 256 R¹³ R¹ G⁶ 257 R¹⁴ R¹G⁶ 258 R¹⁵ R¹ G⁶ 259 R¹⁶ R¹ G⁶ 260 R¹⁷ R¹ G⁶ 261 R¹⁸ R¹ G⁶ 262 R¹⁹ R¹ G⁶263 R²⁰ R¹ G⁶ 264 R²¹ R¹ G⁶ 265 R²² R¹ G⁶ 266 R²³ R¹ G⁶ 267 R²⁴ R¹ G⁶268 R²⁵ R¹ G⁶ 269 R²⁶ R¹ G⁶ 270 R²⁷ R¹ G⁶ 271 R²⁸ R¹ G⁶ 272 R²⁹ R¹ G⁶273 R³⁰ R¹ G⁶ 274 R³¹ R¹ G⁶ 275 R³² R¹ G⁶ 276 R¹ R² G⁶ 277 R¹ R³ G⁶ 278R¹ R⁴ G⁶ 279 R¹ R⁵ G⁶ 280 R¹ R⁶ G⁶ 281 R¹ R⁷ G⁶ 282 R¹ R⁸ G⁶ 283 R¹ R⁹G⁶ 284 R¹ R¹⁰ G⁶ 285 R¹ R¹¹ G⁶ 286 R¹ R¹² G⁶ 287 R¹ R¹³ G⁶ 288 R¹ R¹⁴ G⁶289 R¹ R¹⁵ G⁶ 290 R¹ R¹⁶ G⁶ 291 R¹ R¹⁷ G⁶ 292 R¹ R¹⁸ G⁶ 293 R¹ R¹⁹ G⁶294 R¹ R²⁰ G⁶ 295 R¹ R²¹ G⁶ 296 R¹ R²² G⁶ 297 R¹ R²³ G⁶ 298 R¹ R²⁴ G⁶299 R¹ R²⁵ G⁶ 300 R¹ R²⁶ G⁶ 301 R¹ R²⁷ G⁶ 302 R¹ R²⁸ G⁶ 303 R¹ R²⁹ G⁶304 R¹ R³⁰ G⁶ 305 R¹ R³¹ G⁶ 306 R¹ R³² G⁶ 307 R³ R² G⁶ 308 R⁴ R² G⁶ 309R⁵ R² G⁶ 310 R⁶ R² G⁶ 311 R⁷ R² G⁶ 312 R⁸ R² G⁶ 313 R⁹ R² G⁶ 314 R¹⁰ R²G⁶ 315 R¹¹ R² G⁶ 316 R¹² R² G⁶ 317 R¹³ R² G⁶ 318 R¹⁴ R² G⁶ 319 R¹⁵ R² G⁶320 R¹⁶ R² G⁶ 321 R¹⁷ R² G⁶ 322 R¹⁸ R² G⁶ 323 R¹⁹ R² G⁶ 324 R²⁰ R² G⁶325 R²¹ R² G⁶ 326 R²² R² G⁶ 327 R²³ R² G⁶ 328 R²⁴ R² G⁶ 329 R²⁵ R² G⁶330 R²⁶ R² G⁶ 331 R²⁷ R² G⁶ 332 R²⁸ R² G⁶ 333 R²⁹ R² G⁶ 334 R³⁰ R² G⁶335 R³¹ R² G⁶ 336 R³² R² G⁶ 337 R² R³ G⁶ 338 R² R⁴ G⁶ 339 R² R⁵ G⁶ 340R² R⁶ G⁶ 341 R² R⁷ G⁶ 342 R² R⁸ G⁶ 343 R² R⁹ G⁶ 344 R² R¹⁰ G⁶ 345 R² R¹¹G⁶ 346 R² R¹² G⁶ 347 R² R¹³ G⁶ 348 R² R¹⁴ G⁶ 349 R² R¹⁵ G⁶ 350 R² R¹⁶ G⁶351 R² R¹⁷ G⁶ 352 R² R¹⁸ G⁶ 353 R² R¹⁹ G⁶ 354 R² R²⁰ G⁶ 355 R² R²¹ G⁶356 R² R²² G⁶ 357 R² R²³ G⁶ 358 R² R²⁴ G⁶ 359 R² R²⁵ G⁶ 360 R² R²⁶ G⁶361 R² R²⁷ G⁶ 362 R² R²⁸ G⁶ 363 R² R²⁹ G⁶ 364 R² R³⁰ G⁶ 365 R² R³¹ G⁶366 R² R³² G⁶ 367 R² R³² G⁶ 368 R³ R³² G⁶ 369 R⁴ R³² G⁶ 370 R⁵ R³² G⁶371 R⁶ R³² G⁶ 372 R⁷ R³² G⁶ 373 R⁸ R³² G⁶ 374 R⁹ R³² G⁶ 375 R¹⁰ R³² G⁶376 R¹¹ R³² G⁶ 377 R¹² R³² G⁶ 378 R¹³ R³² G⁶ 379 R¹⁴ R³² G⁶ 380 R¹⁵ R³²G⁶ 381 R¹⁶ R³² G⁶ 382 R¹⁷ R³² G⁶ 383 R¹⁸ R³² G⁶ 384 R¹⁹ R³² G⁶ 385 R²⁰R³² G⁶ 386 R²¹ R³² G⁶ 387 R²² R³² G⁶ 388 R²³ R³² G⁶ 389 R²⁴ R³² G⁶ 390R²⁵ R³² G⁶ 391 R²⁶ R³² G⁶ 392 R²⁷ R³² G⁶ 393 R²⁸ R³² G⁶ 394 R²⁹ R³² G⁶395 R³⁰ R³² G⁶ 396 R³¹ R³² G⁶ 397 R³² R² G⁶ 398 R³² R³ G⁶ 399 R³² R⁴ G⁶400 R³² R⁵ G⁶ 401 R³² R⁶ G⁶ 402 R³² R⁷ G⁶ 403 R³² R⁸ G⁶ 404 R³² R⁹ G⁶405 R³² R¹⁰ G⁶ 406 R³² R¹¹ G⁶ 407 R³² R¹² G⁶ 408 R³² R¹³ G⁶ 409 R³² R¹⁴G⁶ 410 R³² R¹⁵ G⁶ 411 R³² R¹⁶ G⁶ 412 R³² R¹⁷ G⁶ 413 R³² R¹⁸ G⁶ 414 R³²R¹⁹ G⁶ 415 R³² R²⁰ G⁶ 416 R³² R²¹ G⁶ 417 R³² R²² G⁶ 418 R³² R²³ G⁶ 419R³² R²⁴ G⁶ 420 R³² R²⁵ G⁶ 421 R³² R²⁶ G⁶ 422 R³² R²⁷ G⁶ 423 R³² R²⁸ G⁶424 R³² R²⁹ G⁶ 425 R³² R³⁰ G⁶ 426 R³² R³¹ G⁶ 427 R¹ R³³ G⁵ 428 R¹ R³⁴ G⁵429 R¹ R³⁵ G⁵ 430 R¹ R³⁶ G⁵ 431 R¹ R³⁷ G⁵ 432 R¹ R³⁸ G⁵ 433 R¹ R³⁹ G⁵434 R¹ R⁴⁰ G⁵ 435 R¹ R⁴¹ G⁵ 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508 R¹ R² G⁸ 509 R¹ R³ G⁸ 510R¹ R⁴ G⁸ 511 R¹ R⁵ G⁸ 512 R¹ R⁶ G⁸ 513 R¹ R⁷ G⁸ 514 R¹ R⁸ G⁸ 515 R¹ R⁹G⁸ 516 R¹ R¹⁰ G⁸ 517 R¹ R¹¹ G⁸ 518 R¹ R¹² G⁸ 519 R¹ R¹³ G⁸ 520 R¹ R¹⁴ G⁸521 R¹ R¹⁵ G⁸ 522 R¹ R¹⁶ G⁸ 523 R¹ R¹⁷ G⁸ 524 R¹ R¹⁸ G⁸ 525 R¹ R¹⁹ G⁸526 R¹ R²⁰ G⁸ 527 R¹ R²¹ G⁸ 528 R¹ R²² G⁸ 529 R¹ R²³ G⁸ 530 R¹ R²⁴ G⁸531 R¹ R²⁵ G⁸ 532 R¹ R²⁶ G⁸ 533 R¹ R²⁷ G⁸ 534 R¹ R²⁸ G⁸ 535 R¹ R²⁹ G⁸536 R¹ R³⁰ G⁸ 537 R¹ R³¹ G⁸ 538 R¹ R³² G⁸ 539 R³ R² G⁸ 540 R⁴ R² G⁸ 541R⁵ R² G⁸ 542 R⁶ R² G⁸ 543 R⁷ R² G⁸ 544 R⁸ R² G⁸ 545 R⁹ R² G⁸ 546 R¹⁰ R²G⁸ 547 R¹¹ R² G⁸ 548 R¹² R² G⁸ 549 R¹³ R² G⁸ 550 R¹⁴ R² G⁸ 551 R¹⁵ R² G⁸552 R¹⁶ R² G⁸ 553 R¹⁷ R² G⁸ 554 R¹⁸ R² G⁸ 555 R¹⁹ R² G⁸ 556 R²⁰ R² G⁸557 R²¹ R² G⁸ 558 R²² R² G⁸ 559 R²³ R² G⁸ 560 R²⁴ R² G⁸ 561 R²⁵ R² G⁸562 R²⁶ R² G⁸ 563 R²⁷ R² G⁸ 564 R²⁸ R² G⁸ 565 R²⁹ R² G⁸ 566 R³⁰ R² G⁸567 R³¹ R² G⁸ 568 R³² R² G⁸ 569 R² R³ G⁸ 570 R² R⁴ G⁸ 571 R² R⁵ G⁸ 572R² R⁶ G⁸ 573 R² R⁷ G⁸ 574 R² R⁸ G⁸ 575 R² R⁹ G⁸ 576 R² R¹⁰ G⁸ 577 R² R¹¹G⁸ 578 R² R¹² G⁸ 579 R² R¹³ G⁸ 580 R² R¹⁴ G⁸ 581 R² R¹⁵ G⁸ 582 R² R¹⁶ G⁸583 R² R¹⁷ G⁸ 584 R² R¹⁸ G⁸ 585 R² R¹⁹ G⁸ 586 R² R²⁰ G⁸ 587 R² R²¹ G⁸588 R² R²² G⁸ 589 R² R²³ G⁸ 590 R² R²⁴ G⁸ 591 R² R²⁵ G⁸ 592 R² R²⁶ G⁸593 R² R²⁷ G⁸ 594 R² R²⁸ G⁸ 595 R² R²⁹ G⁸ 596 R² R³⁰ G⁸ 597 R² R³¹ G⁸598 R² R³² G⁸ 599 R² R³² G⁸ 600 R³ R³² G⁸ 601 R⁴ R³² G⁸ 602 R⁵ R³² G⁸603 R⁶ R³² G⁸ 604 R⁷ R³² G⁸ 605 R⁸ R³² G⁸ 606 R⁹ R³² G⁸ 607 R¹⁰ R³² G⁸608 R¹¹ R³² G⁸ 609 R¹² R³² G⁸ 610 R¹³ R³² G⁸ 611 R¹⁴ R³² G⁸ 612 R¹⁵ R³²G⁸ 613 R¹⁶ R³² G⁸ 614 R¹⁷ R³² G⁸ 615 R¹⁸ R³² G⁸ 616 R¹⁹ R³² G⁸ 617 R²⁰R³² G⁸ 618 R²¹ R³² G⁸ 619 R²² R³² G⁸ 620 R²³ R³² G⁸ 621 R²⁴ R³² G⁸ 622R²⁵ R³² G⁸ 623 R²⁶ R³² G⁸ 624 R²⁷ R³² G⁸ 625 R²⁸ R³² G⁸ 626 R²⁹ R³² G⁸627 R³⁰ R³² G⁸ 628 R³¹ R³² G⁸ 629 R³² R² G⁸ 630 R³² R³ G⁸ 631 R³² R⁴ G⁸632 R³² R⁵ G⁸ 633 R³² R⁶ G⁸ 634 R³² R⁷ G⁸ 635 R³² R⁸ G⁸ 636 R³² R⁹ G⁸637 R³² R¹⁰ G⁸ 638 R³² R¹¹ G⁸ 639 R³² R¹² G⁸ 640 R³² R¹³ G⁸ 641 R³² R¹⁴G⁸ 642 R³² R¹⁵ G⁸ 643 R³² R¹⁶ G⁸ 644 R³² R¹⁷ G⁸ 645 R³² R¹⁸ G⁸ 646 R³²R¹⁹ G⁸ 647 R³² R²⁰ G⁸ 648 R³² R²¹ G⁸ 649 R³² R²² G⁸ 650 R³² R²³ G⁸ 651R³² R²⁴ 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R¹ R³ G⁹ 724 R¹ R⁴ G⁹ 725 R¹ R⁵ G⁹ 726 R¹ R⁶G⁹ 727 R¹ R⁷ G⁹ 728 R¹ R⁸ G⁹ 729 R¹ R⁹ G⁹ 730 R¹ R¹⁰ G⁹ 731 R¹ R¹¹ G⁹732 R¹ R¹² G⁹ 733 R¹ R¹³ G⁹ 734 R¹ R¹⁴ G⁹ 735 R¹ R¹⁵ G⁹ 736 R¹ R¹⁶ G⁹737 R¹ R¹⁷ G⁹ 738 R¹ R¹⁸ G⁹ 739 R¹ R¹⁹ G⁹ 740 R¹ R²⁰ G⁹ 741 R¹ R²¹ G⁹742 R¹ R²² G⁹ 743 R¹ R²³ G⁹ 744 R¹ R²⁴ G⁹ 745 R¹ R²⁵ G⁹ 746 R¹ R²⁶ G⁹747 R¹ R²⁷ G⁹ 748 R¹ R²⁸ G⁹ 749 R¹ R²⁹ G⁹ 750 R¹ R³⁰ G⁹ 751 R¹ R³¹ G⁹752 R¹ R³² G⁹ 753 R³ R² G⁹ 754 R⁴ R² G⁹ 755 R⁵ R² G⁹ 756 R⁶ R² G⁹ 757 R⁷R² G⁹ 758 R⁸ R² G⁹ 759 R⁹ R² G⁹ 760 R¹⁰ R² G⁹ 761 R¹¹ R² G⁹ 762 R¹² R²G⁹ 763 R¹³ R² G⁹ 764 R¹⁴ R² G⁹ 765 R¹⁵ R² G⁹ 766 R¹⁶ R² G⁹ 767 R¹⁷ R² G⁹768 R¹⁸ R² G⁹ 769 R¹⁹ R² G⁹ 770 R²⁰ R² G⁹ 771 R²¹ R² G⁹ 772 R²² R² G⁹773 R²³ R² G⁹ 774 R²⁴ R² G⁹ 775 R²⁵ R² G⁹ 776 R²⁶ R² G⁹ 777 R²⁷ R² G⁹778 R²⁸ R² G⁹ 779 R²⁹ R² G⁹ 780 R³⁰ R² G⁹ 781 R³¹ R² G⁹ 782 R³² R² G⁹783 R² R³ G⁹ 784 R² R⁴ G⁹ 785 R² R⁵ G⁹ 786 R² R⁶ G⁹ 787 R² R⁷ G⁹ 788 R²R⁸ G⁹ 789 R² R⁹ G⁹ 790 R² R¹⁰ G⁹ 791 R² R¹¹ G⁹ 792 R² R¹² G⁹ 793 R² R¹³G⁹ 794 R² R¹⁴ G⁹ 795 R² R¹⁵ G⁹ 796 R² R¹⁶ G⁹ 797 R² R¹⁷ G⁹ 798 R² R¹⁸ G⁹799 R² R¹⁹ G⁹ 800 R² R²⁰ G⁹ 801 R² R²¹ G⁹ 802 R² R²² G⁹ 803 R² R²³ G⁹804 R² R²⁴ G⁹ 805 R² R²⁵ G⁹ 806 R² R²⁶ G⁹ 807 R² R²⁷ G⁹ 808 R² R²⁸ G⁹809 R² R²⁹ G⁹ 810 R² R³⁰ G⁹ 811 R² R³¹ G⁹ 812 R² R³² G⁹ 813 R² R³² G⁹814 R³ R³² G⁹ 815 R⁴ R³² G⁹ 816 R⁵ R³² G⁹ 817 R⁶ R³² G⁹ 818 R⁷ R³² G⁹819 R⁸ R³² G⁹ 820 R⁹ R³² G⁹ 821 R¹⁰ R³² G⁹ 822 R¹¹ R³² G⁹ 823 R¹² R³² G⁹824 R¹³ R³² G⁹ 825 R¹⁴ R³² G⁹ 826 R¹⁵ R³² G⁹ 827 R¹⁶ R³² G⁹ 828 R¹⁷ R³²G⁹ 829 R¹⁸ R³² G⁹ 830 R¹⁹ R³² G⁹ 831 R²⁰ R³² G⁹ 832 R²¹ R³² G⁹ 833 R²²R³² G⁹ 834 R²³ R³² G⁹ 835 R²⁴ R³² G⁹ 836 R²⁵ R³² G⁹ 837 R²⁶ R³² G⁹ 838R²⁷ R³² G⁹ 839 R²⁸ R³² G⁹ 840 R²⁹ R³² G⁹ 841 R³⁰ R³² G⁹ 842 R³¹ R³² G⁹843 R³² R² G⁹ 844 R³² R³ G⁹ 845 R³² R⁴ G⁹ 846 R³² R⁵ G⁹ 847 R³² R⁶ G⁹848 R³² R⁷ G⁹ 849 R³² R⁸ G⁹ 850 R³² R⁹ G⁹ 851 R³² R¹⁰ G⁹ 852 R³² R¹¹ G⁹853 R³² R¹² G⁹ 854 R³² R¹³ G⁹ 855 R³² R¹⁴ G⁹ 856 R³² R¹⁵ G⁹ 857 R³² R¹⁶G⁹ 858 R³² R¹⁷ G⁹ 859 R³² R¹⁸ G⁹ 860 R³² R¹⁹ G⁹ 861 R³² R²⁰ G⁹ 862 R³²R²¹ G⁹ 863 R³² R²² G⁹ 864 R³² R²³ G⁹ 865 R³² R²⁴ G⁹ 866 R³² R²⁵ G⁹ 867R³² R²⁶ G⁹ 868 R³² R²⁷ G⁹ 869 R³² R²⁸ G⁹ 870 R³² R²⁹ G⁹ 871 R³² R³⁰ G⁹872 R³² R³¹ G⁹ 873 R¹ R³³ G¹¹ 874 R¹ R³⁴ G¹¹ 875 R¹ R³⁵ G¹¹ 876 R¹ R³⁶G¹¹ 877 R¹ R³⁷ G¹¹ 878 R¹ R³⁸ G¹¹ 879 R¹ R³⁹ G¹¹ 880 R¹ R⁴⁰ G¹¹ 881 R¹R⁴¹ G¹¹ 882 R³³ R¹ G¹¹ 883 R³⁴ R¹ G¹¹ 884 R³⁵ R¹ G¹¹ 885 R³⁶ R¹ G¹¹ 886R³⁷ R¹ G¹¹ 887 R³⁸ R¹ G¹¹ 888 R³⁹ R¹ G¹¹ 889 R⁴⁰ R¹ G¹¹ 890 R⁴¹ R¹ G¹¹891 R¹ R¹ G¹¹ 892 R² R² G¹¹ 893 R³ R³ G¹¹ 894 R⁴ R⁴ G¹¹ 895 R⁵ R⁵ G¹¹896 R⁶ R⁶ G¹¹ 897 R⁷ R⁷ G¹¹ 898 R⁸ R⁸ G¹¹ 899 R⁹ R⁹ G¹¹ 900 R¹⁰ R¹⁰ G¹¹901 R¹¹ R¹¹ G¹¹ 902 R¹² R¹² G¹¹ 903 R¹³ R¹³ G¹¹ 904 R¹⁴ R¹⁴ G¹¹ 905 R¹⁵R¹⁵ G¹¹ 906 R¹⁶ R¹⁶ G¹¹ 907 R¹⁷ R¹⁷ G¹¹ 908 R¹⁸ R¹⁸ G¹¹ 909 R¹⁹ R¹⁹ G¹¹910 R²⁰ R²⁰ G¹¹ 911 R²¹ R²¹ G¹¹ 912 R²² R²² G¹¹ 913 R²³ R²³ G¹¹ 914 R²⁴R²⁴ G¹¹ 915 R²⁵ R²⁵ G¹¹ 916 R²⁶ R²⁶ G¹¹ 917 R²⁷ R²⁷ G¹¹ 918 R²⁸ R²⁸ G¹¹919 R²⁹ R²⁹ G¹¹ 920 R³⁰ R³⁰ G¹¹ 921 R³¹ R³¹ G¹¹ 922 R³² R³² G¹¹ 923 R²R¹ G¹¹ 924 R³ R¹ G¹¹ 925 R⁴ R¹ G¹¹ 926 R⁵ R¹ G¹¹ 927 R⁶ R¹ G¹¹ 928 R⁷ R¹G¹¹ 929 R⁸ R¹ G¹¹ 930 R⁹ R¹ G¹¹ 931 R¹⁰ R¹ G¹¹ 932 R¹¹ R¹ G¹¹ 933 R¹² R¹G¹¹ 934 R¹³ R¹ G¹¹ 935 R¹⁴ R¹ G¹¹ 936 R¹⁵ R¹ G¹¹ 937 R¹⁶ R¹ G¹¹ 938 R¹⁷R¹ G¹¹ 939 R¹⁸ R¹ G¹¹ 940 R¹⁹ R¹ G¹¹ 941 R²⁰ R¹ G¹¹ 942 R²¹ R¹ G¹¹ 943R²² R¹ G¹¹ 944 R²³ R¹ G¹¹ 945 R²⁴ R¹ G¹¹ 946 R²⁵ R¹ G¹¹ 947 R²⁶ R¹ G¹¹948 R²⁷ R¹ G¹¹ 949 R²⁸ R¹ G¹¹ 950 R²⁹ R¹ G¹¹ 951 R³⁰ R¹ G¹¹ 952 R³¹ R¹G¹¹ 953 R³² R¹ G¹¹ 954 R¹ R² G¹¹ 955 R¹ R³ G¹¹ 956 R¹ R⁴ G¹¹ 957 R¹ R⁵G¹¹ 958 R¹ R⁶ G¹¹ 959 R¹ R⁷ G¹¹ 960 R¹ R⁸ G¹¹ 961 R¹ R⁹ G¹¹ 962 R¹ R¹⁰G¹¹ 963 R¹ R¹¹ G¹¹ 964 R¹ R¹² G¹¹ 965 R¹ R¹³ G¹¹ 966 R¹ R¹⁴ G¹¹ 967 R¹R¹⁵ G¹¹ 968 R¹ R¹⁶ G¹¹ 969 R¹ R¹⁷ G¹¹ 970 R¹ R¹⁸ G¹¹ 971 R¹ R¹⁹ G¹¹ 972R¹ R²⁰ G¹¹ 973 R¹ R²¹ G¹¹ 974 R¹ R²² G¹¹ 975 R¹ R²³ G¹¹ 976 R¹ R²⁴ G¹¹977 R¹ R²⁵ G¹¹ 978 R¹ R²⁶ G¹¹ 979 R¹ R²⁷ G¹¹ 980 R¹ R²⁸ G¹¹ 981 R¹ R²⁹G¹¹ 982 R¹ R³⁰ G¹¹ 983 R¹ R³¹ G¹¹ 984 R¹ R³² G¹¹ 985 R³ R² G¹¹ 986 R⁴ R²G¹¹ 987 R⁵ R² G¹¹ 988 R⁶ R² G¹¹ 989 R⁷ R² G¹¹ 990 R⁸ R² G¹¹ 991 R⁹ R²G¹¹ 992 R¹⁰ R² G¹¹ 993 R¹¹ R² G¹¹ 994 R¹² R² G¹¹ 995 R¹³ R² G¹¹ 996 R¹⁴R² G¹¹ 997 R¹⁵ R² G¹¹ 998 R¹⁶ R² G¹¹ 999 R¹⁷ R² G¹¹ 1000 R¹⁸ R² G¹¹ 1001R¹⁹ R² G¹¹ 1002 R²⁰ R² G¹¹ 1003 R²¹ R² G¹¹ 1004 R²² R² G¹¹ 1005 R²³ R²G¹¹ 1006 R²⁴ R² G¹¹ 1007 R²⁵ R² G¹¹ 1008 R²⁶ R² G¹¹ 1009 R²⁷ R² G¹¹ 1010R²⁸ R² G¹¹ 1011 R²⁹ R² G¹¹ 1012 R³⁰ R² G¹¹ 1013 R³¹ R² G¹¹ 1014 R³² R²G¹¹ 1015 R² R³ G¹¹ 1016 R² R⁴ G¹¹ 1017 R² R⁵ G¹¹ 1018 R² R⁶ G¹¹ 1019 R²R⁷ G¹¹ 1020 R² R⁸ G¹¹ 1021 R² R⁹ G¹¹ 1022 R² R¹⁰ G¹¹ 1023 R² R¹¹ G¹¹1024 R² R¹² G¹¹ 1025 R² R¹³ G¹¹ 1026 R² R¹⁴ G¹¹ 1027 R² R¹⁵ G¹¹ 1028 R²R¹⁶ G¹¹ 1029 R² R¹⁷ G¹¹ 1030 R² R¹⁸ G¹¹ 1031 R² R¹⁹ G¹¹ 1032 R² R²⁰ G¹¹1033 R² R²¹ G¹¹ 1034 R² R²² G¹¹ 1035 R² R²³ G¹¹ 1036 R² R²⁴ G¹¹ 1037 R²R²⁵ G¹¹ 1038 R² R²⁶ G¹¹ 1039 R² R²⁷ G¹¹ 1040 R² R²⁸ G¹¹ 1041 R² R²⁹ G¹¹1042 R² R³⁰ G¹¹ 1043 R² R³¹ G¹¹ 1044 R² R³² G¹¹ 1045 R² R³² G¹¹ 1046 R³R³² G¹¹ 1047 R⁴ R³² G¹¹ 1048 R⁵ R³² G¹¹ 1049 R⁶ R³² G¹¹ 1050 R⁷ R³² G¹¹1051 R⁸ R³² G¹¹ 1052 R⁹ R³² G¹¹ 1053 R¹⁰ R³² G¹¹ 1054 R¹¹ R³² G¹¹ 1055R¹² R³² G¹¹ 1056 R¹³ R³² G¹¹ 1057 R¹⁴ R³² G¹¹ 1058 R¹⁵ R³² G¹¹ 1059 R¹⁶R³² G¹¹ 1060 R¹⁷ R³² G¹¹ 1061 R¹⁸ R³² G¹¹ 1062 R¹⁹ R³² G¹¹ 1063 R²⁰ R³²G¹¹ 1064 R²¹ R³² G¹¹ 1065 R²² R³² G¹¹ 1066 R²³ R³² G¹¹ 1067 R²⁴ R³² G¹¹1068 R²⁵ R³² G¹¹ 1069 R²⁶ R³² G¹¹ 1070 R²⁷ R³² G¹¹ 1071 R²⁸ R³² G¹¹ 1072R²⁹ R³² G¹¹ 1073 R³⁰ R³² G¹¹ 1074 R³¹ R³² G¹¹ 1075 R³² R² G¹¹ 1076 R³²R³ G¹¹ 1077 R³² R⁴ G¹¹ 1078 R³² R⁵ G¹¹ 1079 R³² R⁶ G¹¹ 1080 R³² R⁷ G¹¹1081 R³² R⁸ G¹¹ 1082 R³² R⁹ G¹¹ 1083 R³² R¹⁰ G¹¹ 1084 R³² R¹¹ G¹¹ 1085R³² R¹² G¹¹ 1086 R³² R¹³ G¹¹ 1087 R³² R¹⁴ G¹¹ 1088 R³² R¹⁵ G¹¹ 1089 R³²R¹⁶ G¹¹ 1090 R³² R¹⁷ G¹¹ 1091 R³² R¹⁸ G¹¹ 1092 R³² R¹⁹ G¹¹ 1093 R³² R²⁰G¹¹ 1094 R³² R²¹ G¹¹ 1095 R³² R²² G¹¹ 1096 R³² R²³ G¹¹ 1097 R³² R²⁴ G¹¹1098 R³² R²⁵ G¹¹ 1099 R³² R²⁶ G¹¹ 1100 R³² R²⁷ G¹¹ 1101 R³² R²⁸ G¹¹ 1102R³² R²⁹ G¹¹ 1103 R³² R³⁰ G¹¹ 1104 R³² R³¹ G¹¹ 1105 R¹ R¹ G¹³ 1106 R² R²G¹³ 1107 R³ R³ G¹³ 1108 R⁴ R⁴ G¹³ 1109 R⁵ R⁵ G¹³ 1110 R⁶ R⁶ G¹³ 1111 R⁷R⁷ G¹³ 1112 R⁸ R⁸ G¹³ 1113 R⁹ R⁹ G¹³ 1114 R¹⁰ R¹⁰ G¹³ 1115 R¹¹ R¹¹ G¹³1116 R¹² R¹² G¹³ 1117 R¹³ R¹³ G¹³ 1118 R¹⁴ R¹⁴ G¹³ 1119 R¹⁵ R¹⁵ G¹³ 1120R¹⁶ R¹⁶ G¹³ 1121 R¹⁷ R¹⁷ G¹³ 1122 R¹⁸ R¹⁸ G¹³ 1123 R¹⁹ R¹⁹ G¹³ 1124 R²⁰R²⁰ G¹³ 1125 R²¹ R²¹ G¹³ 1126 R²² R²² G¹³ 1127 R²³ R²³ G¹³ 1128 R²⁴ R²⁴G¹³ 1129 R²⁵ R²⁵ G¹³ 1130 R²⁶ R²⁶ G¹³ 1131 R²⁷ R²⁷ G¹³ 1132 R²⁸ R²⁸ G¹³1133 R²⁹ R²⁹ G¹³ 1134 R³⁰ R³⁰ G¹³ 1135 R³¹ R³¹ G¹³ 1136 R³² R³² G¹³ 1137R² R¹ G¹³ 1138 R³ R¹ G¹³ 1139 R⁴ R¹ G¹³ 1140 R⁵ R¹ G¹³ 1141 R⁶ R¹ G¹³1142 R⁷ R¹ G¹³ 1143 R⁸ R¹ G¹³ 1144 R⁹ R¹ G¹³ 1145 R¹⁰ R¹ G¹³ 1146 R¹¹ R¹G¹³ 1147 R¹² R¹ G¹³ 1148 R¹³ R¹ G¹³ 1149 R¹⁴ R¹ G¹³ 1150 R¹⁵ R¹ G¹³ 1151R¹⁶ R¹ G¹³ 1152 R¹⁷ R¹ G¹³ 1153 R¹⁸ R¹ G¹³ 1154 R¹⁹ R¹ G¹³ 1155 R²⁰ R¹G¹³ 1156 R²¹ R¹ G¹³ 1157 R²² R¹ G¹³ 1158 R²³ R¹ G¹³ 1159 R²⁴ R¹ G¹³ 1160R²⁵ R¹ G¹³ 1161 R²⁶ R¹ G¹³ 1162 R²⁷ R¹ G¹³ 1163 R²⁸ R¹ G¹³ 1164 R²⁹ R¹G¹³ 1165 R³⁰ R¹ G¹³ 1166 R³¹ R¹ G¹³ 1167 R³² R¹ G¹³ 1168 R¹ R² G¹³ 1169R¹ R³ G¹³ 1170 R¹ R⁴ G¹³ 1171 R¹ R⁵ G¹³ 1172 R¹ R⁶ G¹³ 1173 R¹ R⁷ G¹³1174 R¹ R⁸ G¹³ 1175 R¹ R⁹ G¹³ 1176 R¹ R¹⁰ G¹³ 1177 R¹ R¹¹ G¹³ 1178 R¹R¹² G¹³ 1179 R¹ R¹³ G¹³ 1180 R¹ R¹⁴ G¹³ 1181 R¹ R¹⁵ G¹³ 1182 R¹ R¹⁶ G¹³1183 R¹ R¹⁷ G¹³ 1184 R¹ R¹⁸ G¹³ 1185 R¹ R¹⁹ G¹³ 1186 R¹ R²⁰ G¹³ 1187 R¹R²¹ G¹³ 1188 R¹ R²² G¹³ 1189 R¹ R²³ G¹³ 1190 R¹ R²⁴ G¹³ 1191 R¹ R²⁵ G¹³1192 R¹ R²⁶ G¹³ 1193 R¹ R²⁷ G¹³ 1194 R¹ R²⁸ G¹³ 1195 R¹ R²⁹ G¹³ 1196 R¹R³⁰ G¹³ 1197 R¹ R³¹ G¹³ 1198 R¹ R³² G¹³ 1199 R³ R² G¹³ 1200 R⁴ R² G¹³1201 R⁵ R² G¹³ 1202 R⁶ R² G¹³ 1203 R⁷ R² G¹³ 1204 R⁸ R² G¹³ 1205 R⁹ R²G¹³ 1206 R¹⁰ R² G¹³ 1207 R¹¹ R² G¹³ 1208 R¹² R² G¹³ 1209 R¹³ R² G¹³ 1210R¹⁴ R² G¹³ 1211 R¹⁵ R² G¹³ 1212 R¹⁶ R² G¹³ 1213 R¹⁷ R² G¹³ 1214 R¹⁸ R²G¹³ 1215 R¹⁹ R² G¹³ 1216 R²⁰ R² G¹³ 1217 R²¹ R² G¹³ 1218 R²² R² G¹³ 1219R²³ R² G¹³ 1220 R²⁴ R² G¹³ 1221 R²⁵ R² G¹³ 1222 R²⁶ R² G¹³ 1223 R²⁷ R²G¹³ 1224 R²⁸ R² G¹³ 1225 R²⁹ R² G¹³ 1226 R³⁰ R² G¹³ 1227 R³¹ R² G¹³ 1228R³² R² G¹³ 1229 R² R³ G¹³ 1230 R² R⁴ G¹³ 1231 R² R⁵ G¹³ 1232 R² R⁶ G¹³1233 R² R⁷ G¹³ 1234 R² R⁸ G¹³ 1235 R² R⁹ G¹³ 1236 R² R¹⁰ G¹³ 1237 R² R¹¹G¹³ 1238 R² R¹² G¹³ 1239 R² R¹³ G¹³ 1240 R² R¹⁴ G¹³ 1241 R² R¹⁵ G¹³ 1242R² R¹⁶ G¹³ 1243 R² R¹⁷ G¹³ 1244 R² R¹⁸ G¹³ 1245 R² R¹⁹ G¹³ 1246 R² R²⁰G¹³ 1247 R² R²¹ G¹³ 1248 R² R²² G¹³ 1249 R² R²³ G¹³ 1250 R² R²⁴ G¹³ 1251R² R²⁵ G¹³ 1252 R² R²⁶ G¹³ 1253 R² R²⁷ G¹³ 1254 R² R²⁸ G¹³ 1255 R² R²⁹G¹³ 1256 R² R³⁰ G¹³ 1257 R² R³¹ G¹³ 1258 R² R³² G¹³ 1259 R² R³² G¹³ 1260R³ R³² G¹³ 1261 R⁴ R³² G¹³ 1262 R⁵ R³² G¹³ 1263 R⁶ R³² G¹³ 1264 R⁷ R³²G¹³ 1265 R⁸ R³² G¹³ 1266 R⁹ R³² G¹³ 1267 R¹⁰ R³² G¹³ 1268 R¹¹ R³² G¹³1269 R¹² R³² G¹³ 1270 R¹³ R³² G¹³ 1271 R¹⁴ R³² G¹³ 1272 R¹⁵ R³² G¹³ 1273R¹⁶ R³² G¹³ 1274 R¹⁷ R³² G¹³ 1275 R¹⁸ R³² G¹³ 1276 R¹⁹ R³² G¹³ 1277 R²⁰R³² G¹³ 1278 R²¹ R³² G¹³ 1279 R²² R³² G¹³ 1280 R²³ R³² G¹³ 1281 R²⁴ R³²G¹³ 1282 R²⁵ R³² G¹³ 1283 R²⁶ R³² G¹³ 1284 R²⁷ R³² G¹³ 1285 R²⁸ R³² G¹³1286 R²⁹ R³² G¹³ 1287 R³⁰ R³² G¹³ 1288 R³¹ R³² G¹³ 1289 R³² R² G¹³ 1290R³² R³ G¹³ 1291 R³² R⁴ G¹³ 1292 R³² R⁵ G¹³ 1293 R³² R⁶ G¹³ 1294 R³² R⁷G¹³ 1295 R³² R⁸ G¹³ 1296 R³² R⁹ G¹³ 1297 R³² R¹⁰ G¹³ 1298 R³² R¹¹ G¹³1299 R³² R¹² G¹³ 1300 R³² R¹³ G¹³ 1301 R³² R¹⁴ G¹³ 1302 R³² R¹⁵ G¹³ 1303R³² R¹⁶ G¹³ 1304 R³² R¹⁷ G¹³ 1305 R³² R¹⁸ G¹³ 1306 R³² R¹⁹ G¹³ 1307 R³²R²⁰ G¹³ 1308 R³² R²¹ G¹³ 1309 R³² R²² G¹³ 1310 R³² R²³ G¹³ 1311 R³² R²⁴G¹³ 1312 R³² R²⁵ G¹³ 1313 R³² R²⁶ G¹³ 1314 R³² R²⁷ G¹³ 1315 R³² R²⁸ G¹³1316 R³² R²⁹ G¹³ 1317 R³² R³⁰ G¹³ 1318 R³² R³¹ G¹³ 1319 R¹ R³³ G¹¹ 1320R¹ R³⁴ G¹¹ 1321 R¹ R³⁵ G¹¹ 1322 R¹ R³⁶ G¹¹ 1323 R¹ R³⁷ G¹¹ 1324 R¹ R³⁸G¹¹ 1325 R¹ R³⁹ G¹¹ 1326 R¹ R⁴⁰ G¹¹ 1327 R¹ R⁴¹ G¹¹ 1328 R³³ R¹ G¹¹ 1329R³⁴ R¹ G¹¹ 1330 R³⁵ R¹ G¹¹ 1331 R³⁶ R¹ G¹¹ 1332 R³⁷ R¹ G¹¹ 1333 R³⁸ R¹G¹¹ 1334 R³⁹ R¹ G¹¹ 1335 R⁴⁰ R¹ G¹¹ 1336 R⁴¹ R¹ G¹¹where R_(E) and R_(F) have the following structures:

wherein G¹ to G¹⁴ have the following structures:

In some embodiments of the compound where the compound has a formula ofM(L_(A))_(p)(L_(B))_(q)(L_(C))_(r) wherein L_(B) and L_(C) are each abidentate ligand; and wherein p is 1, 2, or 3; q is 0, 1, or 2; r is 0,1, or 2; and p+q+r is the oxidation state of the metal M, L_(B) andL_(C) can each be independently selected from the group consisting ofthe Ligand Group C:

where:each Y¹ to Y¹³ are independently selected from the group consisting ofcarbon and nitrogen; Y′ is selected from the group consisting of BR_(e),NR_(e), PR_(e), O, S, Se, C═O, S═O, SO₂, CR_(e)R_(f), SiR_(e)R_(f), andGeR_(e)R_(f);R_(e) and R_(f) can be fused or joined to form a ring;each R_(a), R_(b), R_(c), and R_(d) independently represent zero, mono,or up to a maximum allowed substitution to its associated ring; each ofR_(a), R_(b), R_(c), R_(d), R_(e) and R_(f) is independently a hydrogenor a substituent selected from the group consisting of the generalsubstituents defined herein; and two adjacent substituents of R_(a),R_(b), R_(c), and R_(d) can be fused or joined to form a ring or form amultidentate ligand.

In some embodiments of the compound where the compound has a formula ofM(L_(A))_(p)(L_(B))_(q)(L_(C))^(r) wherein L_(B) and L_(C) are each abidentate ligand; and wherein p is 1, 2, or 3; q is 0, 1, or 2; r is 0,1, or 2; and p+q+r is the oxidation state of the metal M, L_(B) andL_(C) can each be independently selected from the group consisting ofthe Ligand Group D:

In some embodiments, the compound is selected from the group consistingof:

In some embodiments, the compound is selected from the group consistingof:

In another aspect, the compound is selected from the group consistingof:

According to an aspect of the present disclosure, a compound comprisinga ligand L_(A) of the Formula IA

is disclosed, where Ring B represents a five- or six-membered aromaticring; R³ represents from none to the maximum possible number ofsubstitutions;X¹, X², X³, and X⁴ are each independently a CR or N; wherein:

(1) at least two adjacent ones of X¹, X², X³, and X⁴ are CR and fusedinto a five or six-membered aromatic ring, or

(2) at least one of X¹, X², X³, and X⁴ is nitrogen, or

(3) both (1) and (2) are true;

wherein (a) R¹ is CR¹¹R¹²R¹³ or join with R² to form into a ring; or

-   -   (b) R² is not hydrogen; or    -   (c) both (a) and (b) are true;    -   wherein each of R, R¹, R², R³, R¹¹, R¹², and R¹³ is        independently selected from the group consisting of hydrogen,        deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl,        alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl,        heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl,        carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl,        sulfonyl, phosphino, and combinations thereof;    -   any two substituents among R, R¹, R², R³, R¹¹, R¹², and R¹³ are        optionally joined to form into a ring;    -   L_(A) is coordinated to a metal M;    -   L_(A) is optionally linked with other ligands to comprise a        tridentate, tetradentate, pentadentate, or hexadentate ligand;        and    -   M is optionally coordinated to other ligands.

In some embodiments of Formula IA, each of R, R¹, R², R³, R¹¹, R¹², andR¹³ is independently selected from the group consisting of hydrogen,deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy,amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl,nitrile, isonitrile, and combinations thereof.

In some embodiments of Formula IA, each of R, R¹, R², R³, R¹¹, R¹², andR¹³ is independently selected from the group consisting of hydrogen,deuterium, fluorine, alkyl, cycloalkyl, and combinations thereof.

In some embodiments of Formula IA, M is selected from the groupconsisting of Ir, Rh, Re, Ru, Os, Pt, Au, and Cu. In some embodiments, Mis Ir or Pt.

In some embodiments of Formula IA, at least one of X¹, X², X³, and X⁴ isnitrogen.

In some embodiments of Formula IA, R¹ is tert-butyl or substitutedtert-butyl. In some embodiments of the compound, R¹ and R² form into anaromatic ring, which can be further substituted.

In some embodiments of Formula IA, Ring B is phenyl.

In some embodiments of Formula IA, the ligand L_(A) is selected from thegroup consisting of:

where each of R¹, R², R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹², R¹³, R¹⁴,R¹⁵, R¹⁶, R¹⁷, R¹⁸, and R¹⁹ is independently selected from the groupconsisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl,heteroalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl,heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylicacid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl,phosphino, and combinations thereof; wherein any two substituents areoptionally joined to form into a ring.

In some embodiments of Formula IA, each of R¹, R², R⁴, R⁵, R⁶, R⁷, R⁸,R⁹, R¹⁰, R¹¹, R¹², R¹³, R¹⁴, R¹⁵, R¹⁶, R¹⁷, R¹⁸, and R¹⁹ isindependently selected from the group consisting of hydrogen, deuterium,fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl,alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile,isonitrile, and combinations thereof; where any two substituents areoptionally joined to form into a ring.

In some embodiments of Formula IA, each of R¹, R², R⁴, R⁵, R⁶, R⁷, R⁸,R⁹, R¹⁰, R¹¹, R¹², R¹³, R¹⁴, R¹⁵, R¹⁶, R¹⁷, R¹⁸, and R¹⁹ isindependently selected from the group consisting of hydrogen, deuterium,fluorine, alkyl, cycloalkyl, and combinations thereof; wherein any twosubstituents are optionally joined to form into a ring.

In some embodiments of Formula IA, the ligand L_(A) is selected from thegroup

ligands I-L_(Ai) that are based on a structure of Formula I

ligands II-L_(Ai) that are based on a structure of Formula II

ligands III-L_(Ai) that are based on a structure of Formula III

ligands IV-L_(Ai) that are based on a structure of Formula IV

ligands V-L_(Ai) that are based on a structure of Formula V

ligands VI-L_(Ai) that are based on a structure of Formula VI

ligands VII-L_(Ai) that are based on a structure of Formula VII

ligands VIII-L_(Ai) that are based on a structure of Formula VI II

ligands XIX-L_(Ai) that are based on a structure of Formula XIX

ligands X-L_(Ai) that are based on a structure of Formula

ligands XI-L_(Ai) that are based on a structure of Formula XI

ligands XII-L_(Ai) that are based on a structure of Formula XII

wherein i is an integer from 1 to 618 and for each i, R¹, R⁴, R⁵, and R⁶in the formula I, II, III, IV, V, VI, VII, VIII, XIX, X, XI, and XII aredefined as follows:

L_(Ai) R¹ R⁴ R⁵ R⁶ L_(A1) R_(B3) H H H L_(A2) R_(B3) R_(B1) H H L_(A3)R_(B3) R_(B3) H H L_(A4) R_(B3) R_(B4) H H L_(A5) R_(B3) R_(B5) H HL_(A6) R_(B3) R_(B6) H H L_(A7) R_(B3) R_(B7) H H L_(A8) R_(B3) R_(B24)H H L_(A9) R_(B3) R_(B25) H H L_(A10) R_(B3) R_(A3) H H L_(A11) R_(B3)R_(A34) H H L_(A12) R_(B3) R_(A44) H H L_(A13) R_(B3) R_(A52) H HL_(A14) R_(B3) R_(A53) H H L_(A15) R_(B3) R_(A54) H H L_(A16) R_(B3)R_(C3) H H L_(A17) R_(B3) R_(C4) H H L_(A18) R_(B3) R_(C8) H H L_(A19)R_(B3) H R_(B1) H L_(A20) R_(B3) H R_(B3) H L_(A21) R_(B3) H R_(B4) HL_(A22) R_(B3) H R_(B5) H L_(A23) R_(B3) H R_(B6) H L_(A24) R_(B3) HR_(B7) H L_(A25) R_(B3) H R_(B24) H L_(A26) R_(B3) H R_(B25) H L_(A27)R_(B3) H R_(A3) H L_(A28) R_(B3) H R_(A34) H L_(A29) R_(B3) H R_(A44) HL_(A30) R_(B3) H R_(A52) H L_(A31) R_(B3) H R_(A53) H L_(A32) R_(B3) HR_(A54) H L_(A33) R_(B3) H R_(C3) H L_(A34) R_(B3) H R_(C4) H L_(A35)R_(B3) H R_(C8) H L_(A36) R_(B3) R_(B1) R_(B1) H L_(A37) R_(B3) R_(B3)R_(B1) H L_(A38) R_(B3) R_(B4) R_(B1) H L_(A39) R_(B3) R_(B5) R_(B1) HL_(A40) R_(B3) R_(B6) R_(B1) H L_(A41) R_(B3) R_(B7) R_(B1) H L_(A42)R_(B3) R_(B24) R_(B1) H L_(A43) R_(B3) R_(B25) R_(B1) H L_(A44) R_(B3)R_(A3) R_(B1) H L_(A45) R_(B3) R_(A34) R_(B1) H L_(A46) R_(B3) R_(A44)R_(B1) H L_(A47) R_(B3) R_(A52) R_(B1) H L_(A48) R_(B3) R_(A53) R_(B1) HL_(A49) R_(B3) R_(A54) R_(B1) H L_(A50) R_(B3) R_(C3) R_(B1) H L_(A51)R_(B3) R_(C4) R_(B1) H L_(A52) R_(B3) R_(C8) R_(B1) H L_(A53) R_(B3)R_(B1) R_(B1) H L_(A54) R_(B3) R_(B1) R_(B3) H L_(A55) R_(B3) R_(B1)R_(B4) H L_(A56) R_(B3) R_(B1) R_(B5) H L_(A57) R_(B3) R_(B1) R_(B6) HL_(A58) R_(B3) R_(B1) R_(B7) H L_(A59) R_(B3) R_(B1) R_(B24) H L_(A60)R_(B3) R_(B1) R_(B25) H L_(A61) R_(B3) R_(B1) R_(A3) H L_(A62) R_(B3)R_(B1) R_(A34) H L_(A63) R_(B3) R_(B1) R_(A44) H L_(A64) R_(B3) R_(B1)R_(A52) H L_(A65) R_(B3) R_(B1) R_(A53) H L_(A66) R_(B3) R_(B1) R_(A54)H L_(A67) R_(B3) R_(B1) R_(C3) H L_(A68) R_(B3) R_(B1) R_(C4) H L_(A69)R_(B3) R_(B1) R_(C8) H L_(A70) R_(B3) R_(B1) R_(B1) R_(B1) L_(A71)R_(B3) R_(B1) R_(B3) R_(B1) L_(A72) R_(B3) R_(B1) R_(B4) R_(B1) L_(A73)R_(B3) R_(B1) R_(B5) R_(B1) L_(A74) R_(B3) R_(B1) R_(B6) R_(B1) L_(A75)R_(B3) R_(B1) R_(B7) R_(B1) L_(A76) R_(B3) R_(B1) R_(B24) R_(B1) L_(A77)R_(B3) R_(B1) R_(B25) R_(B1) L_(A78) R_(B3) R_(B1) R_(A3) R_(B1) L_(A79)R_(B3) R_(B1) R_(A34) R_(B1) L_(A80) R_(B3) R_(B1) R_(A44) R_(B1)L_(A81) R_(B3) R_(B1) R_(A52) R_(B1) L_(A82) R_(B3) R_(B1) R_(A53)R_(B1) L_(A83) R_(B3) R_(B1) R_(A54) R_(B1) L_(A84) R_(B3) R_(B1) R_(C3)R_(B1) L_(A85) R_(B3) R_(B1) R_(C4) R_(B1) L_(A86) R_(B3) R_(B1) R_(C8)R_(B1) L_(A87) R_(B3) R_(B1) R_(B1) R_(B1) L_(A88) R_(B3) R_(B3) R_(B1)R_(B1) L_(A89) R_(B3) R_(B4) R_(B1) R_(B1) L_(A90) R_(B3) R_(B5) R_(B1)R_(B1) L_(A91) R_(B3) R_(B6) R_(B1) R_(B1) L_(A92) R_(B3) R_(B7) R_(B1)R_(B1) L_(A93) R_(B3) R_(B24) R_(B1) R_(B1) L_(A94) R_(B3) R_(B25)R_(B1) R_(B1) L_(A95) R_(B3) R_(A3) R_(B1) R_(B1) L_(A96) R_(B3) R_(A34)R_(B1) R_(B1) L_(A97) R_(B3) R_(A44) R_(B1) R_(B1) L_(A98) R_(B3)R_(A52) R_(B1) R_(B1) L_(A99) R_(B3) R_(A53) R_(B1) R_(B1) L_(A100)R_(B3) R_(A54) R_(B1) R_(B1) L_(A101) R_(B3) R_(C3) R_(B1) R_(B1)L_(A102) R_(B3) R_(C4) R_(B1) R_(B1) L_(A103) R_(B3) R_(C8) R_(B1)R_(B1) L_(A104) R_(B6) H H H L_(A105) R_(B6) R_(B1) H H L_(A106) R_(B6)R_(B3) H H L_(A107) R_(B6) R_(B4) H H L_(A108) R_(B6) R_(B5) H HL_(A109) R_(B6) R_(B6) H H L_(A110) R_(B6) R_(B7) H H L_(A111) R_(B6)R_(B24) H H L_(A112) R_(B6) R_(B25) H H L_(A113) R_(B6) R_(A3) H HL_(A114) R_(B6) R_(A34) H H L_(A115) R_(B6) R_(A44) H H L_(A116) R_(B6)R_(A52) H H L_(A117) R_(B6) R_(A53) H H L_(A118) R_(B6) R_(A54) H HL_(A119) R_(B6) R_(C3) H H L_(A120) R_(B6) R_(C4) H H L_(A121) R_(B6)R_(C8) H H L_(A122) R_(B6) H R_(B1) H L_(A123) R_(B6) H R_(B3) HL_(A124) R_(B6) H R_(B4) H L_(A125) R_(B6) H R_(B5) H L_(A126) R_(B6) HR_(B6) H L_(A127) R_(B6) H R_(B7) H L_(A128) R_(B6) H R_(B24) H L_(A129)R_(B6) H R_(B25) H L_(A130) R_(B6) H R_(A3) H L_(A131) R_(B6) H R_(A34)H L_(A132) R_(B6) H R_(A44) H L_(A133) R_(B6) H R_(A52) H L_(A134)R_(B6) H R_(A53) H L_(A135) R_(B6) H R_(A54) H L_(A136) R_(B6) H R_(C3)H L_(A137) R_(B6) H R_(C4) H L_(A138) R_(B6) H R_(C8) H L_(A139) R_(B6)R_(B1) R_(B1) H L_(A140) R_(B6) R_(B3) R_(B1) H L_(A141) R_(B6) R_(B4)R_(B1) H L_(A142) R_(B6) R_(B5) R_(B1) H L_(A143) R_(B6) R_(B6) R_(B1) HL_(A144) R_(B6) R_(B7) R_(B1) H L_(A145) R_(B6) R_(B24) R_(B1) HL_(A146) R_(B6) R_(B25) R_(B1) H L_(A147) R_(B6) R_(A3) R_(B1) HL_(A148) R_(B6) R_(A34) R_(B1) H L_(A149) R_(B6) R_(A44) R_(B1) HL_(A150) R_(B6) R_(A52) R_(B1) H L_(A151) R_(B6) R_(A53) R_(B1) HL_(A152) R_(B6) R_(A54) R_(B1) H L_(A153) R_(B6) R_(C3) R_(B1) HL_(A154) R_(B6) R_(C4) R_(B1) H L_(A155) R_(B6) R_(C8) R_(B1) H L_(A156)R_(B6) R_(B1) R_(B1) H L_(A157) R_(B6) R_(B1) R_(B3) H L_(A158) R_(B6)R_(B1) R_(B4) H L_(A159) R_(B6) R_(B1) R_(B5) H L_(A160) R_(B6) R_(B1)R_(B6) H L_(A161) R_(B6) R_(B1) R_(B7) H L_(A162) R_(B6) R_(B1) R_(B24)H L_(A163) R_(B6) R_(B1) R_(B25) H L_(A164) R_(B6) R_(B1) R_(A3) HL_(A165) R_(B6) R_(B1) R_(A34) H L_(A166) R_(B6) R_(B1) R_(A44) HL_(A167) R_(B6) R_(B1) R_(A52) H L_(A168) R_(B6) R_(B1) R_(A53) HL_(A169) R_(B6) R_(B1) R_(A54) H L_(A170) R_(B6) R_(B1) R_(C3) HL_(A171) R_(B6) R_(B1) R_(C4) H L_(A172) R_(B6) R_(B1) R_(C8) H L_(A173)R_(B6) R_(B1) R_(B1) R_(B1) L_(A174) R_(B6) R_(B1) R_(B3) R_(B1)L_(A175) R_(B6) R_(B1) R_(B4) R_(B1) L_(A176) R_(B6) R_(B1) R_(B5)R_(B1) L_(A177) R_(B6) R_(B1) R_(B6) R_(B1) L_(A178) R_(B6) R_(B1)R_(B7) R_(B1) L_(A179) R_(B6) R_(B1) R_(B24) R_(B1) L_(A180) R_(B6)R_(B1) R_(B25) R_(B1) L_(A181) R_(B6) R_(B1) R_(A3) R_(B1) L_(A182)R_(B6) R_(B1) R_(A34) R_(B1) L_(A183) R_(B6) R_(B1) R_(A44) R_(B1)L_(A184) R_(B6) R_(B1) R_(A52) R_(B1) L_(A185) R_(B6) R_(B1) R_(A53)R_(B1) L_(A186) R_(B6) R_(B1) R_(A54) R_(B1) L_(A187) R_(B6) R_(B1)R_(C3) R_(B1) L_(A188) R_(B6) R_(B1) R_(C4) R_(B1) L_(A189) R_(B6)R_(B1) R_(C8) R_(B1) L_(A190) R_(B6) R_(B1) R_(B1) R_(B1) L_(A191)R_(B6) R_(B3) R_(B1) R_(B1) L_(A192) R_(B6) R_(B4) R_(B1) R_(B1)L_(A193) R_(B6) R_(B5) R_(B1) R_(B1) L_(A194) R_(B6) R_(B6) R_(B1)R_(B1) L_(A195) R_(B6) R_(B7) R_(B1) R_(B1) L_(A196) R_(B6) R_(B24)R_(B1) R_(B1) L_(A197) R_(B6) R_(B25) R_(B1) R_(B1) L_(A198) R_(B6)R_(A3) R_(B1) R_(B1) L_(A199) R_(B6) R_(A34) R_(B1) R_(B1) L_(A200)R_(B6) R_(A44) R_(B1) R_(B1) L_(A201) R_(B6) R_(A52) R_(B1) R_(B1)L_(A202) R_(B6) R_(A53) R_(B1) R_(B1) L_(A203) R_(B6) R_(A54) R_(B1)R_(B1) L_(A204) R_(B6) R_(C3) R_(B1) R_(B1) L_(A205) R_(B6) R_(C4)R_(B1) R_(B1) L_(A206) R_(B6) R_(C8) R_(B1) R_(B1) L_(A207) R_(B7) H H HL_(A208) R_(B7) R_(B1) H H L_(A209) R_(B7) R_(B3) H H L_(A210) R_(B7)R_(B4) H H L_(A211) R_(B7) R_(B5) H H L_(A212) R_(B7) R_(B6) H HL_(A213) R_(B7) R_(B7) H H L_(A214) R_(B7) R_(B24) H H L_(A215) R_(B7)R_(B25) H H L_(A216) R_(B7) R_(A3) H H L_(A217) R_(B7) R_(A34) H HL_(A218) R_(B7) R_(A44) H H L_(A219) R_(B7) R_(A52) H H L_(A220) R_(B7)R_(A53) H H L_(A221) R_(B7) R_(A54) H H L_(A222) R_(B7) R_(C3) H HL_(A223) R_(B7) R_(C4) H H L_(A224) R_(B7) R_(C8) H H L_(A225) R_(B7) HR_(B1) H L_(A226) R_(B7) H R_(B3) H L_(A227) R_(B7) H R_(B4) H L_(A228)R_(B7) H R_(B5) H L_(A229) R_(B7) H R_(B6) H L_(A230) R_(B7) H R_(B7) HL_(A231) R_(B7) H R_(B24) H L_(A232) R_(B7) H R_(B25) H L_(A233) R_(B7)H R_(A3) H L_(A234) R_(B7) H R_(A34) H L_(A235) R_(B7) H R_(A44) HL_(A236) R_(B7) H R_(A52) H L_(A237) R_(B7) H R_(A53) H L_(A238) R_(B7)H R_(A54) H L_(A239) R_(B7) H R_(C3) H L_(A240) R_(B7) H R_(C4) HL_(A241) R_(B7) H R_(C8) H L_(A242) R_(B7) R_(B1) R_(B1) H L_(A243)R_(B7) R_(B3) R_(B1) H L_(A244) R_(B7) R_(B4) R_(B1) H L_(A245) R_(B7)R_(B5) R_(B1) H L_(A246) R_(B7) R_(B6) R_(B1) H L_(A247) R_(B7) R_(B7)R_(B1) H L_(A248) R_(B7) R_(B24) R_(B1) H L_(A249) R_(B7) R_(B25) R_(B1)H L_(A250) R_(B7) R_(A3) R_(B1) H L_(A251) R_(B7) R_(A34) R_(B1) HL_(A252) R_(B7) R_(A44) R_(B1) H L_(A253) R_(B7) R_(A52) R_(B1) HL_(A254) R_(B7) R_(A53) R_(B1) H L_(A255) R_(B7) R_(A54) R_(B1) HL_(A256) R_(B7) R_(C3) R_(B1) H L_(A257) R_(B7) R_(C4) R_(B1) H L_(A258)R_(B7) R_(C8) R_(B1) H L_(A259) R_(B7) R_(B1) R_(B1) H L_(A260) R_(B7)R_(B1) R_(B3) H L_(A261) R_(B7) R_(B1) R_(B4) H L_(A262) R_(B7) R_(B1)R_(B5) H L_(A263) R_(B7) R_(B1) R_(B6) H L_(A264) R_(B7) R_(B1) R_(B7) HL_(A265) R_(B7) R_(B1) R_(B24) H L_(A266) R_(B7) R_(B1) R_(B25) HL_(A267) R_(B7) R_(B1) R_(A3) H L_(A268) R_(B7) R_(B1) R_(A34) HL_(A269) R_(B7) R_(B1) R_(A44) H L_(A270) R_(B7) R_(B1) R_(A52) HL_(A271) R_(B7) R_(B1) R_(A53) H L_(A272) R_(B7) R_(B1) R_(A54) HL_(A273) R_(B7) R_(B1) R_(C3) H L_(A274) R_(B7) R_(B1) R_(C4) H L_(A275)R_(B7) R_(B1) R_(C8) H L_(A276) R_(B7) R_(B1) R_(B1) R_(B1) L_(A277)R_(B7) R_(B1) R_(B3) R_(B1) L_(A278) R_(B7) R_(B1) R_(B4) R_(B1)L_(A279) R_(B7) R_(B1) R_(B5) R_(B1) L_(A280) R_(B7) R_(B1) R_(B6)R_(B1) L_(A281) R_(B7) R_(B1) R_(B7) R_(B1) L_(A282) R_(B7) R_(B1)R_(B24) R_(B1) L_(A283) R_(B7) R_(B1) R_(B25) R_(B1) L_(A284) R_(B7)R_(B1) R_(A3) R_(B1) L_(A285) R_(B7) R_(B1) R_(A34) R_(B1) L_(A286)R_(B7) R_(B1) R_(A44) R_(B1) L_(A287) R_(B7) R_(B1) R_(A52) R_(B1)L_(A288) R_(B7) R_(B1) R_(A53) R_(B1) L_(A289) R_(B7) R_(B1) R_(A54)R_(B1) L_(A290) R_(B7) R_(B1) R_(C3) R_(B1) L_(A291) R_(B7) R_(B1)R_(C4) R_(B1) L_(A292) R_(B7) R_(B1) R_(C8) R_(B1) L_(A293) R_(B7)R_(B1) R_(B1) R_(B1) L_(A294) R_(B7) R_(B3) R_(B1) R_(B1) L_(A295)R_(B7) R_(B4) R_(B1) R_(B1) L_(A296) R_(B7) R_(B5) R_(B1) R_(B1)L_(A297) R_(B7) R_(B6) R_(B1) R_(B1) L_(A298) R_(B7) R_(B7) R_(B1)R_(B1) L_(A299) R_(B7) R_(B24) R_(B1) R_(B1) L_(A300) R_(B7) R_(B25)R_(B1) R_(B1) L_(A301) R_(B7) R_(A3) R_(B1) R_(B1) L_(A302) R_(B7)R_(A34) R_(B1) R_(B1) L_(A303) R_(B7) R_(A44) R_(B1) R_(B1) L_(A304)R_(B7) R_(A52) R_(B1) R_(B1) L_(A305) R_(B7) R_(A53) R_(B1) R_(B1)L_(A306) R_(B7) R_(A54) R_(B1) R_(B1) L_(A307) R_(B7) R_(C3) R_(B1)R_(B1) L_(A308) R_(B7) R_(C4) R_(B1) R_(B1) L_(A309) R_(B7) R_(C8)R_(B1) R_(B1) L_(A310) R_(B9) H H H L_(A311) R_(B9) R_(B1) H H L_(A312)R_(B9) R_(B3) H H L_(A313) R_(B9) R_(B4) H H L_(A314) R_(B9) R_(B5) H HL_(A315) R_(B9) R_(B6) H H L_(A316) R_(B9) R_(B7) H H L_(A317) R_(B9)R_(B24) H H L_(A318) R_(B9) R_(B25) H H L_(A319) R_(B9) R_(A3) H HL_(A320) R_(B9) R_(A34) H H L_(A321) R_(B9) R_(A44) H H L_(A322) R_(B9)R_(A52) H H L_(A323) R_(B9) R_(A53) H H L_(A324) R_(B9) R_(A54) H HL_(A325) R_(B9) R_(C3) H H L_(A326) R_(B9) R_(C4) H H L_(A327) R_(B9)R_(C8) H H L_(A328) R_(B9) H R_(B1) H L_(A329) R_(B9) H R_(B3) HL_(A330) R_(B9) H R_(B4) H L_(A331) R_(B9) H R_(B5) H L_(A332) R_(B9) HR_(B6) H L_(A333) R_(B9) H R_(B7) H L_(A334) R_(B9) H R_(B24) H L_(A335)R_(B9) H R_(B25) H L_(A336) R_(B9) H R_(A3) H L_(A337) R_(B9) H R_(A34)H L_(A338) R_(B9) H R_(A44) H L_(A339) R_(B9) H R_(A52) H L_(A340)R_(B9) H R_(A53) H L_(A341) R_(B9) H R_(A54) H L_(A342) R_(B9) H R_(C3)H L_(A343) R_(B9) H R_(C4) H L_(A344) R_(B9) H R_(C8) H L_(A345) R_(B9)R_(B1) R_(B1) H L_(A346) R_(B9) R_(B3) R_(B1) H L_(A347) R_(B9) R_(B4)R_(B1) H L_(A348) R_(B9) R_(B5) R_(B1) H L_(A349) R_(B9) R_(B6) R_(B1) HL_(A350) R_(B9) R_(B7) R_(B1) H L_(A351) R_(B9) R_(B24) R_(B1) HL_(A352) R_(B9) R_(B25) R_(B1) H L_(A353) R_(B9) R_(A3) R_(B1) HL_(A354) R_(B9) R_(A34) R_(B1) H L_(A355) R_(B9) R_(A44) R_(B1) HL_(A356) R_(B9) R_(A52) R_(B1) H L_(A357) R_(B9) R_(A53) R_(B1) HL_(A358) R_(B9) R_(A54) R_(B1) H L_(A359) R_(B9) R_(C3) R_(B1) HL_(A360) R_(B9) R_(C4) R_(B1) H L_(A361) R_(B9) R_(C8) R_(B1) H L_(A362)R_(B9) R_(B1) R_(B1) H L_(A363) R_(B9) R_(B1) R_(B3) H L_(A364) R_(B9)R_(B1) R_(B4) H L_(A365) R_(B9) R_(B1) R_(B5) H L_(A366) R_(B9) R_(B1)R_(B6) H L_(A367) R_(B9) R_(B1) R_(B7) H L_(A368) R_(B9) R_(B1) R_(B24)H L_(A369) R_(B9) R_(B1) R_(B25) H L_(A370) R_(B9) R_(B1) R_(A3) HL_(A371) R_(B9) R_(B1) R_(A34) H L_(A372) R_(B9) R_(B1) R_(A44) HL_(A373) R_(B9) R_(B1) R_(A52) H L_(A374) R_(B9) R_(B1) R_(A53) HL_(A375) R_(B9) R_(B1) R_(A54) H L_(A376) R_(B9) R_(B1) R_(C3) HL_(A377) R_(B9) R_(B1) R_(C4) H L_(A378) R_(B9) R_(B1) R_(C8) H L_(A379)R_(B9) R_(B1) R_(B1) R_(B1) L_(A380) R_(B9) R_(B1) R_(B3) R_(B1)L_(A381) R_(B9) R_(B1) R_(B4) R_(B1) L_(A382) R_(B9) R_(B1) R_(B5)R_(B1) L_(A383) R_(B9) R_(B1) R_(B6) R_(B1) L_(A384) R_(B9) R_(B1)R_(B7) R_(B1) L_(A385) R_(B9) R_(B1) R_(B24) R_(B1) L_(A386) R_(B9)R_(B1) R_(B25) R_(B1) L_(A387) R_(B9) R_(B1) R_(A3) R_(B1) L_(A388)R_(B9) R_(B1) R_(A34) R_(B1) L_(A389) R_(B9) R_(B1) R_(A44) R_(B1)L_(A390) R_(B9) R_(B1) R_(A52) R_(B1) L_(A391) R_(B9) R_(B1) R_(A53)R_(B1) L_(A392) R_(B9) R_(B1) R_(A54) R_(B1) L_(A393) R_(B9) R_(B1)R_(C3) R_(B1) L_(A394) R_(B9) R_(B1) R_(C4) R_(B1) L_(A395) R_(B9)R_(B1) R_(C8) R_(B1) L_(A396) R_(B9) R_(B1) R_(B1) R_(B1) L_(A397)R_(B9) R_(B3) R_(B1) R_(B1) L_(A398) R_(B9) R_(B4) R_(B1) R_(B1)L_(A399) R_(B9) R_(B5) R_(B1) R_(B1) L_(A400) R_(B9) R_(B6) R_(B1)R_(B1) L_(A401) R_(B9) R_(B7) R_(B1) R_(B1) L_(A402) R_(B9) R_(B24)R_(B1) R_(B1) L_(A403) R_(B9) R_(B25) R_(B1) R_(B1) L_(A404) R_(B9)R_(A3) R_(B1) R_(B1) L_(A405) R_(B9) R_(A34) R_(B1) R_(B1) L_(A406)R_(B9) R_(A44) R_(B1) R_(B1) L_(A407) R_(B9) R_(A52) R_(B1) R_(B1)L_(A408) R_(B9) R_(A53) R_(B1) R_(B1) L_(A409) R_(B9) R_(A54) R_(B1)R_(B1) L_(A410) R_(B9) R_(C3) R_(B1) R_(B1) L_(A411) R_(B9) R_(C4)R_(B1) R_(B1) L_(A412) R_(B9) R_(C8) R_(B1) R_(B1) L_(A413) R_(B15) H HH L_(A414) R_(B15) R_(B1) H H L_(A415) R_(B15) R_(B3) H H L_(A416)R_(B15) R_(B4) H H L_(A417) R_(B15) R_(B5) H H L_(A418) R_(B15) R_(B6) HH L_(A419) R_(B15) R_(B7) H H L_(A420) R_(B15) R_(B24) H H L_(A421)R_(B15) R_(B25) H H L_(A422) R_(B15) R_(A3) H H L_(A423) R_(B15) R_(A34)H H L_(A424) R_(B15) R_(A44) H H L_(A425) R_(B15) R_(A52) H H L_(A426)R_(B15) R_(A53) H H L_(A427) R_(B15) R_(A54) H H L_(A428) R_(B15) R_(C3)H H L_(A429) R_(B15) R_(C4) H H L_(A430) R_(B15) R_(C8) H H L_(A431)R_(B15) H R_(B1) H L_(A432) R_(B15) H R_(B3) H L_(A433) R_(B15) H R_(B4)H L_(A434) R_(B15) H R_(B5) H L_(A435) R_(B15) H R_(B6) H L_(A436)R_(B15) H R_(B7) H L_(A437) R_(B15) H R_(B24) H L_(A438) R_(B15) HR_(B25) H L_(A439) R_(B15) H R_(A3) H L_(A440) R_(B15) H R_(A34) HL_(A441) R_(B15) H R_(A44) H L_(A442) R_(B15) H R_(A52) H L_(A443)R_(B15) H R_(A53) H L_(A444) R_(B15) H R_(A54) H L_(A445) R_(B15) HR_(C3) H L_(A446) R_(B15) H R_(C4) H L_(A447) R_(B15) H R_(C8) HL_(A448) R_(B15) R_(B1) R_(B1) H L_(A449) R_(B15) R_(B3) R_(B1) HL_(A450) R_(B15) R_(B4) R_(B1) H L_(A451) R_(B15) R_(B5) R_(B1) HL_(A452) R_(B15) R_(B6) R_(B1) H L_(A453) R_(B15) R_(B7) R_(B1) HL_(A454) R_(B15) R_(B24) R_(B1) H L_(A455) R_(B15) R_(B25) R_(B1) HL_(A456) R_(B15) R_(A3) R_(B1) H L_(A457) R_(B15) R_(A34) R_(B1) HL_(A458) R_(B15) R_(A44) R_(B1) H L_(A459) R_(B15) R_(A52) R_(B1) HL_(A460) R_(B15) R_(A53) R_(B1) H L_(A461) R_(B15) R_(A54) R_(B1) HL_(A462) R_(B15) R_(C3) R_(B1) H L_(A463) R_(B15) R_(C4) R_(B1) HL_(A464) R_(B15) R_(C8) R_(B1) H L_(A465) R_(B15) R_(B1) R_(B1) HL_(A466) R_(B15) R_(B1) R_(B3) H L_(A467) R_(B15) R_(B1) R_(B4) HL_(A468) R_(B15) R_(B1) R_(B5) H L_(A469) R_(B15) R_(B1) R_(B6) HL_(A470) R_(B15) R_(B1) R_(B7) H L_(A471) R_(B15) R_(B1) R_(B24) HL_(A472) R_(B15) R_(B1) R_(B25) H L_(A473) R_(B15) R_(B1) R_(A3) HL_(A474) R_(B15) R_(B1) R_(A34) H L_(A475) R_(B15) R_(B1) R_(A44) HL_(A476) R_(B15) R_(B1) R_(A52) H L_(A477) R_(B15) R_(B1) R_(A53) HL_(A478) R_(B15) R_(B1) R_(A54) H L_(A479) R_(B15) R_(B1) R_(C3) HL_(A480) R_(B15) R_(B1) R_(C4) H L_(A481) R_(B15) R_(B1) R_(C8) HL_(A482) R_(B15) R_(B1) R_(B1) R_(B1) L_(A483) R_(B15) R_(B1) R_(B3)R_(B1) L_(A484) R_(B15) R_(B1) R_(B4) R_(B1) L_(A485) R_(B15) R_(B1)R_(B5) R_(B1) L_(A486) R_(B15) R_(B1) R_(B6) R_(B1) L_(A487) R_(B15)R_(B1) R_(B7) R_(B1) L_(A488) R_(B15) R_(B1) R_(B24) R_(B1) L_(A489)R_(B15) R_(B1) R_(B25) R_(B1) L_(A490) R_(B15) R_(B1) R_(A3) R_(B1)L_(A491) R_(B15) R_(B1) R_(A34) R_(B1) L_(A492) R_(B15) R_(B1) R_(A44)R_(B1) L_(A493) R_(B15) R_(B1) R_(A52) R_(B1) L_(A494) R_(B15) R_(B1)R_(A53) R_(B1) L_(A495) R_(B15) R_(B1) R_(A54) R_(B1) L_(A496) R_(B15)R_(B1) R_(C3) R_(B1) L_(A497) R_(B15) R_(B1) R_(C4) R_(B1) L_(A498)R_(B15) R_(B1) R_(C8) R_(B1) L_(A499) R_(B15) R_(B1) R_(B1) R_(B1)L_(A500) R_(B15) R_(B3) R_(B1) R_(B1) L_(A501) R_(B15) R_(B4) R_(B1)R_(B1) L_(A502) R_(B15) R_(B5) R_(B1) R_(B1) L_(A503) R_(B15) R_(B6)R_(B1) R_(B1) L_(A504) R_(B15) R_(B7) R_(B1) R_(B1) L_(A505) R_(B15)R_(B24) R_(B1) R_(B1) L_(A506) R_(B15) R_(B25) R_(B1) R_(B1) L_(A507)R_(B15) R_(A3) R_(B1) R_(B1) L_(A508) R_(B15) R_(A34) R_(B1) R_(B1)L_(A509) R_(B15) R_(A44) R_(B1) R_(B1) L_(A510) R_(B15) R_(A52) R_(B1)R_(B1) L_(A511) R_(B15) R_(A53) R_(B1) R_(B1) L_(A512) R_(B15) R_(A54)R_(B1) R_(B1) L_(A513) R_(B15) R_(C3) R_(B1) R_(B1) L_(A514) R_(B15)R_(C4) R_(B1) R_(B1) L_(A515) R_(B15) R_(C8) R_(B1) R_(B1) L_(A516)R_(A44) H H H L_(A517) R_(A44) R_(B1) H H L_(A518) R_(A44) R_(B3) H HL_(A519) R_(A44) R_(B4) H H L_(A520) R_(A44) R_(B5) H H L_(A521) R_(A44)R_(B6) H H L_(A522) R_(A44) R_(B7) H H L_(A523) R_(A44) R_(B24) H HL_(A524) R_(A44) R_(B25) H H L_(A525) R_(A44) R_(A3) H H L_(A526)R_(A44) R_(A34) H H L_(A527) R_(A44) R_(A44) H H L_(A528) R_(A44)R_(A52) H H L_(A529) R_(A44) R_(A53) H H L_(A530) R_(A44) R_(A54) H HL_(A531) R_(A44) R_(C3) H H L_(A532) R_(A44) R_(C4) H H L_(A533) R_(A44)R_(C8) H H L_(A534) R_(A44) H R_(B1) H L_(A535) R_(A44) H R_(B3) HL_(A536) R_(A44) H R_(B4) H L_(A537) R_(A44) H R_(B5) H L_(A538) R_(A44)H R_(B6) H L_(A539) R_(A44) H R_(B7) H L_(A540) R_(A44) H R_(B24) HL_(A541) R_(A44) H R_(B25) H L_(A542) R_(A44) H R_(A3) H L_(A543)R_(A44) H R_(A34) H L_(A544) R_(A44) H R_(A44) H L_(A545) R_(A44) HR_(A52) H L_(A546) R_(A44) H R_(A53) H L_(A547) R_(A44) H R_(A54) HL_(A548) R_(A44) H R_(C3) H L_(A549) R_(A44) H R_(C4) H L_(A550) R_(A44)H R_(C8) H L_(A551) R_(A44) R_(B1) R_(B1) H L_(A552) R_(A44) R_(B3)R_(B1) H L_(A553) R_(A44) R_(B4) R_(B1) H L_(A554) R_(A44) R_(B5) R_(B1)H L_(A555) R_(A44) R_(B6) R_(B1) H L_(A556) R_(A44) R_(B7) R_(B1) HL_(A557) R_(A44) R_(B24) R_(B1) H L_(A558) R_(A44) R_(B25) R_(B1) HL_(A559) R_(A44) R_(A3) R_(B1) H L_(A560) R_(A44) R_(A34) R_(B1) HL_(A561) R_(A44) R_(A44) R_(B1) H L_(A562) R_(A44) R_(A52) R_(B1) HL_(A563) R_(A44) R_(A53) R_(B1) H L_(A564) R_(A44) R_(A54) R_(B1) HL_(A565) R_(A44) R_(C3) R_(B1) H L_(A566) R_(A44) R_(C4) R_(B1) HL_(A567) R_(A44) R_(C8) R_(B1) H L_(A568) R_(A44) R_(B1) R_(B1) HL_(A569) R_(A44) R_(B1) R_(B3) H L_(A570) R_(A44) R_(B1) R_(B4) HL_(A571) R_(A44) R_(B1) R_(B5) H L_(A572) R_(A44) R_(B1) R_(B6) HL_(A573) R_(A44) R_(B1) R_(B7) H L_(A574) R_(A44) R_(B1) R_(B24) HL_(A575) R_(A44) R_(B1) R_(B25) H L_(A576) R_(A44) R_(B1) R_(A3) HL_(A577) R_(A44) R_(B1) R_(A34) H L_(A578) R_(A44) R_(B1) R_(A44) HL_(A579) R_(A44) R_(B1) R_(A52) H L_(A580) R_(A44) R_(B1) R_(A53) HL_(A581) R_(A44) R_(B1) R_(A54) H L_(A582) R_(A44) R_(B1) R_(C3) HL_(A583) R_(A44) R_(B1) R_(C4) H L_(A584) R_(A44) R_(B1) R_(C8) HL_(A585) R_(A44) R_(B1) R_(B1) R_(B1) L_(A586) R_(A44) R_(B1) R_(B3)R_(B1) L_(A587) R_(A44) R_(B1) R_(B4) R_(B1) L_(A588) R_(A44) R_(B1)R_(B5) R_(B1) L_(A589) R_(A44) R_(B1) R_(B6) R_(B1) L_(A590) R_(A44)R_(B1) R_(B7) R_(B1) L_(A591) R_(A44) R_(B1) R_(B24) R_(B1) L_(A592)R_(A44) R_(B1) R_(B25) R_(B1) L_(A593) R_(A44) R_(B1) R_(A3) R_(B1)L_(A594) R_(A44) R_(B1) R_(A34) R_(B1) L_(A595) R_(A44) R_(B1) R_(A44)R_(B1) L_(A596) R_(A44) R_(B1) R_(A52) R_(B1) L_(A597) R_(A44) R_(B1)R_(A53) R_(B1) L_(A598) R_(A44) R_(B1) R_(A54) R_(B1) L_(A599) R_(A44)R_(B1) R_(C3) R_(B1) L_(A600) R_(A44) R_(B1) R_(C4) R_(B1) L_(A601)R_(A44) R_(B1) R_(C8) R_(B1) L_(A602) R_(A44) R_(B1) R_(B1) R_(B1)L_(A603) R_(A44) R_(B3) R_(B1) R_(B1) L_(A604) R_(A44) R_(B4) R_(B1)R_(B1) L_(A605) R_(A44) R_(B5) R_(B1) R_(B1) L_(A606) R_(A44) R_(B6)R_(B1) R_(B1) L_(A607) R_(A44) R_(B7) R_(B1) R_(B1) L_(A608) R_(A44)R_(B24) R_(B1) R_(B1) L_(A609) R_(A44) R_(B25) R_(B1) R_(B1) L_(A610)R_(A44) R_(A3) R_(B1) R_(B1) L_(A611) R_(A44) R_(A34) R_(B1) R_(B1)L_(A612) R_(A44) R_(A44) R_(B1) R_(B1) L_(A613) R_(A44) R_(A52) R_(B1)R_(B1) L_(A614) R_(A44) R_(A53) R_(B1) R_(B1) L_(A615) R_(A44) R_(A54)R_(B1) R_(B1) L_(A616) R_(A44) R_(C3) R_(B1) R_(B1) L_(A617) R_(A44)R_(C4) R_(B1) R_(B1) L_(A618) R_(A44) R_(C8) R_(B1) R_(B1)

In some embodiments of the compound, the first ligand L_(A) is selectedfrom the group consisting of:

ligands XIII-L_(Ai) that are based on a structure of Formula XIII

ligands XIV-L_(Ai) that are based on a structure of Formula XIV

ligands XV-L_(Ai) that are based on a structure of Formula XV

ligands XVI-L_(Ai) that are based on a structure of Formula XVI

ligands XVII-L_(Ai) that are based on a structure of Formula XVII

wherein i is an integer from 619 to 1170 and for each i, R¹, R⁹, R¹⁰,and Y in the formulas XIII, XIV, XV, XVI, and XVII are defined asfollows:

L_(Ai) R¹ R⁹ R¹⁰ Y L_(A619) R_(B6) H H CH L_(A620) R_(B6) R_(B1) H CHL_(A621) R_(B6) R_(B3) H CH L_(A622) R_(B6) R_(B4) H CH L_(A623) R_(B6)R_(B5) H CH L_(A624) R_(B6) R_(B6) H CH L_(A625) R_(B6) R_(B7) H CHL_(A626) R_(B6) R_(B24) H CH L_(A627) R_(B6) R_(B25) H CH L_(A628)R_(B6) R_(A3) H CH L_(A629) R_(B6) R_(A34) H CH L_(A630) R_(B6) R_(A44)H CH L_(A631) R_(B6) R_(A52) H CH L_(A632) R_(B6) R_(A53) H CH L_(A633)R_(B6) R_(A54) H CH L_(A634) R_(B6) R_(C3) H CH L_(A635) R_(B6) R_(C4) HCH L_(A636) R_(B6) R_(C8) H CH L_(A637) R_(B6) H R_(B1) CH L_(A638)R_(B6) H R_(B3) CH L_(A639) R_(B6) H R_(B4) CH L_(A640) R_(B6) H R_(B5)CH L_(A641) R_(B6) H R_(B6) CH L_(A642) R_(B6) H R_(B7) CH L_(A643)R_(B6) H R_(B24) CH L_(A644) R_(B6) H R_(B25) CH L_(A645) R_(B6) HR_(A3) CH L_(A646) R_(B6) H R_(A34) CH L_(A647) R_(B6) H R_(A44) CHL_(A648) R_(B6) H R_(A52) CH L_(A649) R_(B6) H R_(A53) CH L_(A650)R_(B6) H R_(A54) CH L_(A651) R_(B6) H R_(C3) CH L_(A652) R_(B6) H R_(C4)CH L_(A653) R_(B6) H R_(C8) CH L_(A654) R_(B6) R_(B1) R_(B1) CH L_(A655)R_(B6) R_(B3) R_(B1) CH L_(A656) R_(B6) R_(B4) R_(B1) CH L_(A657) R_(B6)R_(B5) R_(B1) CH L_(A658) R_(B6) R_(B6) R_(B1) CH L_(A659) R_(B6) R_(B7)R_(B1) CH L_(A660) R_(B6) R_(B24) R_(B1) CH L_(A661) R_(B6) R_(B25)R_(B1) CH L_(A662) R_(B6) R_(A3) R_(B1) CH L_(A663) R_(B6) R_(A34)R_(B1) CH L_(A664) R_(B6) R_(A44) R_(B1) CH L_(A665) R_(B6) R_(A52)R_(B1) CH L_(A666) R_(B6) R_(A53) R_(B1) CH L_(A667) R_(B6) R_(A54)R_(B1) CH L_(A668) R_(B6) R_(C3) R_(B1) CH L_(A669) R_(B6) R_(C4) R_(B1)CH L_(A670) R_(B6) R_(C8) R_(B1) CH L_(A671) R_(B6) R_(B1) R_(B1) CHL_(A672) R_(B6) R_(B1) R_(B3) CH L_(A673) R_(B6) R_(B1) R_(B4) CHL_(A674) R_(B6) R_(B1) R_(B5) CH L_(A675) R_(B6) R_(B1) R_(B6) CHL_(A676) R_(B6) R_(B1) R_(B7) CH L_(A677) R_(B6) R_(B1) R_(B24) CHL_(A678) R_(B6) R_(B1) R_(B25) CH L_(A679) R_(B6) R_(B1) R_(A3) CHL_(A680) R_(B6) R_(B1) R_(A34) CH L_(A681) R_(B6) R_(B1) R_(A44) CHL_(A682) R_(B6) R_(B1) R_(A52) CH L_(A683) R_(B6) R_(B1) R_(A53) CHL_(A684) R_(B6) R_(B1) R_(A54) CH L_(A685) R_(B6) R_(B1) R_(C3) CHL_(A686) R_(B6) R_(B1) R_(C4) CH L_(A687) R_(B6) R_(B1) R_(C8) CHL_(A688) R_(B7) H H CH L_(A689) R_(B7) R_(B1) H CH L_(A690) R_(B7)R_(B3) H CH L_(A691) R_(B7) R_(B4) H CH L_(A692) R_(B7) R_(B5) H CHL_(A693) R_(B7) R_(B6) H CH L_(A694) R_(B7) R_(B7) H CH L_(A695) R_(B7)R_(B24) H CH L_(A696) R_(B7) R_(B25) H CH L_(A697) R_(B7) R_(A3) H CHL_(A698) R_(B7) R_(A34) H CH L_(A699) R_(B7) R_(A44) H CH L_(A700)R_(B7) R_(A52) H CH L_(A701) R_(B7) R_(A53) H CH L_(A702) R_(B7) R_(A54)H CH L_(A703) R_(B7) R_(C3) H CH L_(A704) R_(B7) R_(C4) H CH L_(A705)R_(B7) R_(C8) H CH L_(A706) R_(B7) H R_(B1) CH L_(A707) R_(B7) H R_(B3)CH L_(A708) R_(B7) H R_(B4) CH L_(A709) R_(B7) H R_(B5) CH L_(A710)R_(B7) H R_(B6) CH L_(A711) R_(B7) H R_(B7) CH L_(A712) R_(B7) H R_(B24)CH L_(A713) R_(B7) H R_(B25) CH L_(A714) R_(B7) H R_(A3) CH L_(A715)R_(B7) H R_(A34) CH L_(A716) R_(B7) H R_(A44) CH L_(A717) R_(B7) HR_(A52) CH L_(A718) R_(B7) H R_(A53) CH L_(A719) R_(B7) H R_(A54) CHL_(A720) R_(B7) H R_(C3) CH L_(A721) R_(B7) H R_(C4) CH L_(A722) R_(B7)H R_(C8) CH L_(A723) R_(B7) R_(B1) R_(B1) CH L_(A724) R_(B7) R_(B3)R_(B1) CH L_(A725) R_(B7) R_(B4) R_(B1) CH L_(A726) R_(B7) R_(B5) R_(B1)CH L_(A727) R_(B7) R_(B6) R_(B1) CH L_(A728) R_(B7) R_(B7) R_(B1) CHL_(A729) R_(B7) R_(B24) R_(B1) CH L_(A730) R_(B7) R_(B25) R_(B1) CHL_(A731) R_(B7) R_(A3) R_(B1) CH L_(A732) R_(B7) R_(A34) R_(B1) CHL_(A733) R_(B7) R_(A44) R_(B1) CH L_(A734) R_(B7) R_(A52) R_(B1) CHL_(A735) R_(B7) R_(A53) R_(B1) CH L_(A736) R_(B7) R_(A54) R_(B1) CHL_(A737) R_(B7) R_(C3) R_(B1) CH L_(A738) R_(B7) R_(C4) R_(B1) CHL_(A739) R_(B7) R_(C8) R_(B1) CH L_(A740) R_(B7) R_(B1) R_(B1) CHL_(A741) R_(B7) R_(B1) R_(B3) CH L_(A742) R_(B7) R_(B1) R_(B4) CHL_(A743) R_(B7) R_(B1) R_(B5) CH L_(A744) R_(B7) R_(B1) R_(B6) CHL_(A745) R_(B7) R_(B1) R_(B7) CH L_(A746) R_(B7) R_(B1) R_(B24) CHL_(A747) R_(B7) R_(B1) R_(B25) CH L_(A748) R_(B7) R_(B1) R_(A3) CHL_(A749) R_(B7) R_(B1) R_(A34) CH L_(A750) R_(B7) R_(B1) R_(A44) CHL_(A751) R_(B7) R_(B1) R_(A52) CH L_(A752) R_(B7) R_(B1) R_(A53) CHL_(A753) R_(B7) R_(B1) R_(A54) CH L_(A754) R_(B7) R_(B1) R_(C3) CHL_(A755) R_(B7) R_(B1) R_(C4) CH L_(A756) R_(B7) R_(B1) R_(C8) CHL_(A757) R_(B9) H H CH L_(A758) R_(B9) R_(B1) H CH L_(A759) R_(B9)R_(B3) H CH L_(A760) R_(B9) R_(B4) H CH L_(A761) R_(B9) R_(B5) H CHL_(A762) R_(B9) R_(B6) H CH L_(A763) R_(B9) R_(B7) H CH L_(A764) R_(B9)R_(B24) H CH L_(A765) R_(B9) R_(B25) H CH L_(A766) R_(B9) R_(A3) H CHL_(A767) R_(B9) R_(A34) H CH L_(A768) R_(B9) R_(A44) H CH L_(A769)R_(B9) R_(A52) H CH L_(A770) R_(B9) R_(A53) H CH L_(A771) R_(B9) R_(A54)H CH L_(A772) R_(B9) R_(C3) H CH L_(A773) R_(B9) R_(C4) H CH L_(A774)R_(B9) R_(C8) H CH L_(A775) R_(B9) H R_(B1) CH L_(A776) R_(B9) H R_(B3)CH L_(A777) R_(B9) H R_(B4) CH L_(A778) R_(B9) H R_(B5) CH L_(A779)R_(B9) H R_(B6) CH L_(A780) R_(B9) H R_(B7) CH L_(A781) R_(B9) H R_(B24)CH L_(A782) R_(B9) H R_(B25) CH L_(A783) R_(B9) H R_(A3) CH L_(A784)R_(B9) H R_(A34) CH L_(A785) R_(B9) H R_(A44) CH L_(A786) R_(B9) HR_(A52) CH L_(A787) R_(B9) H R_(A53) CH L_(A788) R_(B9) H R_(A54) CHL_(A789) R_(B9) H R_(C3) CH L_(A790) R_(B9) H R_(C4) CH L_(A791) R_(B9)H R_(C8) CH L_(A792) R_(B9) R_(B1) R_(B1) CH L_(A793) R_(B9) R_(B3)R_(B1) CH L_(A794) R_(B9) R_(B4) R_(B1) CH L_(A795) R_(B9) R_(B5) R_(B1)CH L_(A796) R_(B9) R_(B6) R_(B1) CH L_(A797) R_(B9) R_(B7) R_(B1) CHL_(A798) R_(B9) R_(B24) R_(B1) CH L_(A799) R_(B9) R_(B25) R_(B1) CHL_(A800) R_(B9) R_(A3) R_(B1) CH L_(A801) R_(B9) R_(A34) R_(B1) CHL_(A802) R_(B9) R_(A44) R_(B1) CH L_(A803) R_(B9) R_(A52) R_(B1) CHL_(A804) R_(B9) R_(A53) R_(B1) CH L_(A805) R_(B9) R_(A54) R_(B1) CHL_(A806) R_(B9) R_(C3) R_(B1) CH L_(A807) R_(B9) R_(C4) R_(B1) CHL_(A808) R_(B9) R_(C8) R_(B1) CH L_(A809) R_(B9) R_(B1) R_(B1) CHL_(A810) R_(B9) R_(B1) R_(B3) CH L_(A811) R_(B9) R_(B1) R_(B4) CHL_(A812) R_(B9) R_(B1) R_(B5) CH L_(A813) R_(B9) R_(B1) R_(B6) CHL_(A814) R_(B9) R_(B1) R_(B7) CH L_(A815) R_(B9) R_(B1) R_(B24) CHL_(A816) R_(B9) R_(B1) R_(B25) CH L_(A817) R_(B9) R_(B1) R_(A3) CHL_(A818) R_(B9) R_(B1) R_(A34) CH L_(A819) R_(B9) R_(B1) R_(A44) CHL_(A820) R_(B9) R_(B1) R_(A52) CH L_(A821) R_(B9) R_(B1) R_(A53) CHL_(A822) R_(B9) R_(B1) R_(A54) CH L_(A823) R_(B9) R_(B1) R_(C3) CHL_(A824) R_(B9) R_(B1) R_(C4) CH L_(A825) R_(B9) R_(B1) R_(C8) CHL_(A826) R_(B44) H H CH L_(A827) R_(B44) R_(B1) H CH L_(A828) R_(B44)R_(B3) H CH L_(A829) R_(B44) R_(B4) H CH L_(A830) R_(B44) R_(B5) H CHL_(A831) R_(B44) R_(B6) H CH L_(A832) R_(B44) R_(B7) H CH L_(A833)R_(B44) R_(B24) H CH L_(A834) R_(B44) R_(B25) H CH L_(A835) R_(B44)R_(A3) H CH L_(A836) R_(B44) R_(A34) H CH L_(A837) R_(B44) R_(A44) H CHL_(A838) R_(B44) R_(A52) H CH L_(A839) R_(B44) R_(A53) H CH L_(A840)R_(B44) R_(A54) H CH L_(A841) R_(B44) R_(C3) H CH L_(A842) R_(B44)R_(C4) H CH L_(A843) R_(B44) R_(C8) H CH L_(A844) R_(B44) H R_(B1) CHL_(A845) R_(B44) H R_(B3) CH L_(A846) R_(B44) H R_(B4) CH L_(A847)R_(B44) H R_(B5) CH L_(A848) R_(B44) H R_(B6) CH L_(A849) R_(B44) HR_(B7) CH L_(A850) R_(B44) H R_(B24) CH L_(A851) R_(B44) H R_(B25) CHL_(A852) R_(B44) H R_(A3) CH L_(A853) R_(B44) H R_(A34) CH L_(A854)R_(B44) H R_(A44) CH L_(A855) R_(B44) H R_(A52) CH L_(A856) R_(B44) HR_(A53) CH L_(A857) R_(B44) H R_(A54) CH L_(A858) R_(B44) H R_(C3) CHL_(A859) R_(B44) H R_(C4) CH L_(A860) R_(B44) H R_(C8) CH L_(A861)R_(B44) R_(B1) R_(B1) CH L_(A862) R_(B44) R_(B3) R_(B1) CH L_(A863)R_(B44) R_(B4) R_(B1) CH L_(A864) R_(B44) R_(B5) R_(B1) CH L_(A865)R_(B44) R_(B6) R_(B1) CH L_(A866) R_(B44) R_(B7) R_(B1) CH L_(A867)R_(B44) R_(B24) R_(B1) CH L_(A868) R_(B44) R_(B25) R_(B1) CH L_(A869)R_(B44) R_(A3) R_(B1) CH L_(A870) R_(B44) R_(A34) R_(B1) CH L_(A871)R_(B44) R_(A44) R_(B1) CH L_(A872) R_(B44) R_(A52) R_(B1) CH L_(A873)R_(B44) R_(A53) R_(B1) CH L_(A874) R_(B44) R_(A54) R_(B1) CH L_(A875)R_(B44) R_(C3) R_(B1) CH L_(A876) R_(B44) R_(C4) R_(B1) CH L_(A877)R_(B44) R_(C8) R_(B1) CH L_(A878) R_(B44) R_(B1) R_(B1) CH L_(A879)R_(B44) R_(B1) R_(B3) CH L_(A880) R_(B44) R_(B1) R_(B4) CH L_(A881)R_(B44) R_(B1) R_(B5) CH L_(A882) R_(B44) R_(B1) R_(B6) CH L_(A883)R_(B44) R_(B1) R_(B7) CH L_(A884) R_(B44) R_(B1) R_(B24) CH L_(A885)R_(B44) R_(B1) R_(B25) CH L_(A886) R_(B44) R_(B1) R_(A3) CH L_(A887)R_(B44) R_(B1) R_(A34) CH L_(A888) R_(B44) R_(B1) R_(A44) CH L_(A889)R_(B44) R_(B1) R_(A52) CH L_(A890) R_(B44) R_(B1) R_(A53) CH L_(A891)R_(B44) R_(B1) R_(A54) CH L_(A892) R_(B44) R_(B1) R_(C3) CH L_(A893)R_(B44) R_(B1) R_(C4) CH L_(A894) R_(B44) R_(B1) R_(C8) CH L_(A895)R_(B6) H H N L_(A896) R_(B6) R_(B1) H N L_(A897) R_(B6) R_(B3) H NL_(A898) R_(B6) R_(B4) H N L_(A899) R_(B6) R_(B5) H N L_(A900) R_(B6)R_(B6) H N L_(A901) R_(B6) R_(B7) H N L_(A902) R_(B6) R_(B24) H NL_(A903) R_(B6) R_(B25) H N L_(A904) R_(B6) R_(A3) H N L_(A905) R_(B6)R_(A34) H N L_(A906) R_(B6) R_(A44) H N L_(A907) R_(B6) R_(A52) H NL_(A908) R_(B6) R_(A53) H N L_(A909) R_(B6) R_(A54) H N L_(A910) R_(B6)R_(C3) H N L_(A911) R_(B6) R_(C4) H N L_(A912) R_(B6) R_(C8) H NL_(A913) R_(B6) H R_(B1) N L_(A914) R_(B6) H R_(B3) N L_(A915) R_(B6) HR_(B4) N L_(A916) R_(B6) H R_(B5) N L_(A917) R_(B6) H R_(B6) N L_(A918)R_(B6) H R_(B7) N L_(A919) R_(B6) H R_(B24) N L_(A920) R_(B6) H R_(B25)N L_(A921) R_(B6) H R_(A3) N L_(A922) R_(B6) H R_(A34) N L_(A923) R_(B6)H R_(A44) N L_(A924) R_(B6) H R_(A52) N L_(A925) R_(B6) H R_(A53) NL_(A926) R_(B6) H R_(A54) N L_(A927) R_(B6) H R_(C3) N L_(A928) R_(B6) HR_(C4) N L_(A929) R_(B6) H R_(C8) N L_(A930) R_(B6) R_(B1) R_(B1) NL_(A931) R_(B6) R_(B3) R_(B1) N L_(A932) R_(B6) R_(B4) R_(B1) N L_(A933)R_(B6) R_(B5) R_(B1) N L_(A934) R_(B6) R_(B6) R_(B1) N L_(A935) R_(B6)R_(B7) R_(B1) N L_(A936) R_(B6) R_(B24) R_(B1) N L_(A937) R_(B6) R_(B25)R_(B1) N L_(A938) R_(B6) R_(A3) R_(B1) N L_(A939) R_(B6) R_(A34) R_(B1)N L_(A940) R_(B6) R_(A44) R_(B1) N L_(A941) R_(B6) R_(A52) R_(B1) NL_(A942) R_(B6) R_(A53) R_(B1) N L_(A943) R_(B6) R_(A54) R_(B1) NL_(A944) R_(B6) R_(C3) R_(B1) N L_(A945) R_(B6) R_(C4) R_(B1) N L_(A946)R_(B6) R_(C8) R_(B1) N L_(A947) R_(B6) R_(B1) R_(B1) N L_(A948) R_(B6)R_(B1) R_(B3) N L_(A949) R_(B6) R_(B1) R_(B4) N L_(A950) R_(B6) R_(B1)R_(B5) N L_(A951) R_(B6) R_(B1) R_(B6) N L_(A952) R_(B6) R_(B1) R_(B7) NL_(A953) R_(B6) R_(B1) R_(B24) N L_(A954) R_(B6) R_(B1) R_(B25) NL_(A955) R_(B6) R_(B1) R_(A3) N L_(A956) R_(B6) R_(B1) R_(A34) NL_(A957) R_(B6) R_(B1) R_(A44) N L_(A958) R_(B6) R_(B1) R_(A52) NL_(A959) R_(B6) R_(B1) R_(A53) N L_(A960) R_(B6) R_(B1) R_(A54) NL_(A961) R_(B6) R_(B1) R_(C3) N L_(A962) R_(B6) R_(B1) R_(C4) N L_(A963)R_(B6) R_(B1) R_(C8) N L_(A964) R_(B7) H H N L_(A965) R_(B7) R_(B1) H NL_(A966) R_(B7) R_(B3) H N L_(A967) R_(B7) R_(B4) H N L_(A968) R_(B7)R_(B5) H N L_(A969) R_(B7) R_(B6) H N L_(A970) R_(B7) R_(B7) H NL_(A971) R_(B7) R_(B24) H N L_(A972) R_(B7) R_(B25) H N L_(A973) R_(B7)R_(A3) H N L_(A974) R_(B7) R_(A34) H N L_(A975) R_(B7) R_(A44) H NL_(A976) R_(B7) R_(A52) H N L_(A977) R_(B7) R_(A53) H N L_(A978) R_(B7)R_(A54) H N L_(A979) R_(B7) R_(C3) H N L_(A980) R_(B7) R_(C4) H NL_(A981) R_(B7) R_(C8) H N L_(A982) R_(B7) H R_(B1) N L_(A983) R_(B7) HR_(B3) N L_(A984) R_(B7) H R_(B4) N L_(A985) R_(B7) H R_(B5) N L_(A986)R_(B7) H R_(B6) N L_(A987) R_(B7) H R_(B7) N L_(A988) R_(B7) H R_(B24) NL_(A989) R_(B7) H R_(B25) N L_(A990) R_(B7) H R_(A3) N L_(A991) R_(B7) HR_(A34) N L_(A992) R_(B7) H R_(A44) N L_(A993) R_(B7) H R_(A52) NL_(A994) R_(B7) H R_(A53) N L_(A995) R_(B7) H R_(A54) N L_(A996) R_(B7)H R_(C3) N L_(A997) R_(B7) H R_(C4) N L_(A998) R_(B7) H R_(C8) NL_(A999) R_(B7) R_(B1) R_(B1) N L_(A1000) R_(B7) R_(B3) R_(B1) NL_(A1001) R_(B7) R_(B4) R_(B1) N L_(A1002) R_(B7) R_(B5) R_(B1) NL_(A1003) R_(B7) R_(B6) R_(B1) N L_(A1004) R_(B7) R_(B7) R_(B1) NL_(A1005) R_(B7) R_(B24) R_(B1) N L_(A1006) R_(B7) R_(B25) R_(B1) NL_(A1007) R_(B7) R_(A3) R_(B1) N L_(A1008) R_(B7) R_(A34) R_(B1) NL_(A1009) R_(B7) R_(A44) R_(B1) N L_(A1010) R_(B7) R_(A52) R_(B1) NL_(A1011) R_(B7) R_(A53) R_(B1) N L_(A1012) R_(B7) R_(A54) R_(B1) NL_(A1013) R_(B7) R_(C3) R_(B1) N L_(A1014) R_(B7) R_(C4) R_(B1) NL_(A1015) R_(B7) R_(C8) R_(B1) N L_(A1016) R_(B7) R_(B1) R_(B1) NL_(A1017) R_(B7) R_(B1) R_(B3) N L_(A1018) R_(B7) R_(B1) R_(B4) NL_(A1019) R_(B7) R_(B1) R_(B5) N L_(A1020) R_(B7) R_(B1) R_(B6) NL_(A1021) R_(B7) R_(B1) R_(B7) N L_(A1022) R_(B7) R_(B1) R_(B24) NL_(A1023) R_(B7) R_(B1) R_(B25) N L_(A1024) R_(B7) R_(B1) R_(A3) NL_(A1025) R_(B7) R_(B1) R_(A34) N L_(A1026) R_(B7) R_(B1) R_(A44) NL_(A1027) R_(B7) R_(B1) R_(A52) N L_(A1028) R_(B7) R_(B1) R_(A53) NL_(A1029) R_(B7) R_(B1) R_(A54) N L_(A1030) R_(B7) R_(B1) R_(C3) NL_(A1031) R_(B7) R_(B1) R_(C4) N L_(A1032) R_(B7) R_(B1) R_(C8) NL_(A1033) R_(B9) H H N L_(A1034) R_(B9) R_(B1) H N L_(A1035) R_(B9)R_(B3) H N L_(A1036) R_(B9) R_(B4) H N L_(A1037) R_(B9) R_(B5) H NL_(A1038) R_(B9) R_(B6) H N L_(A1039) R_(B9) R_(B7) H N L_(A1040) R_(B9)R_(B24) H N L_(A1041) R_(B9) R_(B25) H N L_(A1042) R_(B9) R_(A3) H NL_(A1043) R_(B9) R_(A34) H N L_(A1044) R_(B9) R_(A44) H N L_(A1045)R_(B9) R_(A52) H N L_(A1046) R_(B9) R_(A53) H N L_(A1047) R_(B9) R_(A54)H N L_(A1048) R_(B9) R_(C3) H N L_(A1049) R_(B9) R_(C4) H N L_(A1050)R_(B9) R_(C8) H N L_(A1051) R_(B9) H R_(B1) N L_(A1052) R_(B9) H R_(B3)N L_(A1053) R_(B9) H R_(B4) N L_(A1054) R_(B9) H R_(B5) N L_(A1055)R_(B9) H R_(B6) N L_(A1056) R_(B9) H R_(B7) N L_(A1057) R_(B9) H R_(B24)N L_(A1058) R_(B9) H R_(B25) N L_(A1059) R_(B9) H R_(A3) N L_(A1060)R_(B9) H R_(A34) N L_(A1061) R_(B9) H R_(A44) N L_(A1062) R_(B9) HR_(A52) N L_(A1063) R_(B9) H R_(A53) N L_(A1064) R_(B9) H R_(A54) NL_(A1065) R_(B9) H R_(C3) N L_(A1066) R_(B9) H R_(C4) N L_(A1067) R_(B9)H R_(C8) N L_(A1068) R_(B9) R_(B1) R_(B1) N L_(A1069) R_(B9) R_(B3)R_(B1) N L_(A1070) R_(B9) R_(B4) R_(B1) N L_(A1071) R_(B9) R_(B5) R_(B1)N L_(A1072) R_(B9) R_(B6) R_(B1) N L_(A1073) R_(B9) R_(B7) R_(B1) NL_(A1074) R_(B9) R_(B24) R_(B1) N L_(A1075) R_(B9) R_(B25) R_(B1) NL_(A1076) R_(B9) R_(A3) R_(B1) N L_(A1077) R_(B9) R_(A34) R_(B1) NL_(A1078) R_(B9) R_(A44) R_(B1) N L_(A1079) R_(B9) R_(A52) R_(B1) NL_(A1080) R_(B9) R_(A53) R_(B1) N L_(A1081) R_(B9) R_(A54) R_(B1) NL_(A1082) R_(B9) R_(C3) R_(B1) N L_(A1083) R_(B9) R_(C4) R_(B1) NL_(A1084) R_(B9) R_(C8) R_(B1) N L_(A1085) R_(B9) R_(B1) R_(B1) NL_(A1086) R_(B9) R_(B1) R_(B3) N L_(A1087) R_(B9) R_(B1) R_(B4) NL_(A1088) R_(B9) R_(B1) R_(B5) N L_(A1089) R_(B9) R_(B1) R_(B6) NL_(A1090) R_(B9) R_(B1) R_(B7) N L_(A1091) R_(B9) R_(B1) R_(B24) NL_(A1092) R_(B9) R_(B1) R_(B25) N L_(A1093) R_(B9) R_(B1) R_(A3) NL_(A1094) R_(B9) R_(B1) R_(A34) N L_(A1095) R_(B9) R_(B1) R_(A44) NL_(A1096) R_(B9) R_(B1) R_(A52) N L_(A1097) R_(B9) R_(B1) R_(A53) NL_(A1098) R_(B9) R_(B1) R_(A54) N L_(A1099) R_(B9) R_(B1) R_(C3) NL_(A1100) R_(B9) R_(B1) R_(C4) N L_(A1101) R_(B9) R_(B1) R_(C8) NL_(A1102) R_(B44) H H N L_(A1103) R_(B44) R_(B1) H N L_(A1104) R_(B44)R_(B3) H N L_(A1105) R_(B44) R_(B4) H N L_(A1106) R_(B44) R_(B5) H NL_(A1107) R_(B44) R_(B6) H N L_(A1108) R_(B44) R_(B7) H N L_(A1109)R_(B44) R_(B24) H N L_(A1110) R_(B44) R_(B25) H N L_(A1111) R_(B44)R_(A3) H N L_(A1112) R_(B44) R_(A34) H N L_(A1113) R_(B44) R_(A44) H NL_(A1114) R_(B44) R_(A52) H N L_(A1115) R_(B44) R_(A53) H N L_(A1116)R_(B44) R_(A54) H N L_(A1117) R_(B44) R_(C3) H N L_(A1118) R_(B44)R_(C4) H N L_(A1119) R_(B44) R_(C8) H N L_(A1120) R_(B44) H R_(B1) NL_(A1121) R_(B44) H R_(B3) N L_(A1122) R_(B44) H R_(B4) N L_(A1123)R_(B44) H R_(B5) N L_(A1124) R_(B44) H R_(B6) N L_(A1125) R_(B44) HR_(B7) N L_(A1126) R_(B44) H R_(B24) N L_(A1127) R_(B44) H R_(B25) NL_(A1128) R_(B44) H R_(A3) N L_(A1129) R_(B44) H R_(A34) N L_(A1130)R_(B44) H R_(A44) N L_(A1131) R_(B44) H R_(A52) N L_(A1132) R_(B44) HR_(A53) N L_(A1133) R_(B44) H R_(A54) N L_(A1134) R_(B44) H R_(C3) NL_(A1135) R_(B44) H R_(C4) N L_(A1136) R_(B44) H R_(C8) N L_(A1137)R_(B44) R_(B1) R_(B1) N L_(A1138) R_(B44) R_(B3) R_(B1) N L_(A1139)R_(B44) R_(B4) R_(B1) N L_(A1140) R_(B44) R_(B5) R_(B1) N L_(A1141)R_(B44) R_(B6) R_(B1) N L_(A1142) R_(B44) R_(B7) R_(B1) N L_(A1143)R_(B44) R_(B24) R_(B1) N L_(A1144) R_(B44) R_(B25) R_(B1) N L_(A1145)R_(B44) R_(A3) R_(B1) N L_(A1146) R_(B44) R_(A34) R_(B1) N L_(A1147)R_(B44) R_(A44) R_(B1) N L_(A1148) R_(B44) R_(A52) R_(B1) N L_(A1149)R_(B44) R_(A53) R_(B1) N L_(A1150) R_(B44) R_(A54) R_(B1) N L_(A1151)R_(B44) R_(C3) R_(B1) N L_(A1152) R_(B44) R_(C4) R_(B1) N L_(A1153)R_(B44) R_(C8) R_(B1) N L_(A1154) R_(B44) R_(B1) R_(B1) N L_(A1155)R_(B44) R_(B1) R_(B3) N L_(A1156) R_(B44) R_(B1) R_(B4) N L_(A1157)R_(B44) R_(B1) R_(B5) N L_(A1158) R_(B44) R_(B1) R_(B6) N L_(A1159)R_(B44) R_(B1) R_(B7) N L_(A1160) R_(B44) R_(B1) R_(B24) N L_(A1161)R_(B44) R_(B1) R_(B25) N L_(A1162) R_(B44) R_(B1) R_(A3) N L_(A1163)R_(B44) R_(B1) R_(A34) N L_(A1164) R_(B44) R_(B1) R_(A44) N L_(A1165)R_(B44) R_(B1) R_(A52) N L_(A1166) R_(B44) R_(B1) R_(A53) N L_(A1167)R_(B44) R_(B1) R_(A54) N L_(A1168) R_(B44) R_(B1) R_(C3) N L_(A1169)R_(B44) R_(B1) R_(C4) N L_(A1170) R_(B44) R_(B1) R_(C8) N

In some embodiments of the compound, the first ligand L_(A) is selectedfrom the group consisting of

ligands XVIII-L_(Ai) that are based on a structure of Formula XVIII

ligands XIX-L_(Ai) that are based on a structure of Formula XIX

ligands XX-L_(Ai) that are based on a structure of Formula XX

ligands XXI-L_(Ai) that are based on a structure of Formula XXI

ligands XXII-L_(Ai) that are based on a structure of Formula XXII

ligands XXIII-L_(Ai) that are based on a structure of Formula XXIII

ligands XXIV-L_(Ai) that are based on a structure of Formula XXIV

ligands XXV-L_(Ai) that are based on a structure of Formula XXV

ligands XXVI-L_(Ai) that are based on a structure of Formula XXVI

ligands XXVII-L_(Ai) that are based on a structure of Formula XXVII

ligands XXVIII-L_(Ai) that are based on a structure of Formula XXVIII

ligands XXIX-L_(Ai) that are based on a structure of Formula XXIX

ligands XXX-L_(Ai) that are based on a structure of Formula XXX

ligands XXXI-L_(Ai) that are based on a structure of Formula XXXI

ligands XXXII-L_(Ai) that are based on a structure of Formula XXXII

ligands XXXIII-L_(Ai) that are based on a structure of Formula XXXIII

ligands XXXIV-L_(Ai) that are based on a structure of Formula XXXIV

ligands XXXV-L_(Ai) that are based on a structure of Formula XXXV

ligands XXXVI-L_(Ai) that are based on a structure of Formula XXX VI

ligands XXXVII-L_(Ai) that are based on a structure of Formula XXXVII

ligands XXXVIII-L_(Ai) that are based on a structure of Formula XXXVIII

ligands XXXIX-L_(Ai) that are based on a structure of Formula XXXIX

ligands XL-L_(Ai) that are based on a structure of Formula XL

ligands XLI-L_(Ai) that are based on a structure of Formula XLI

ligands XLII-L_(Ai) that are based on a structure of Formula XLII

ligands XLIII-L_(Ai) that are based on a structure of Formula XLIII

ligands XLIV-L_(Ai) that are based on a structure of Formula XLIV

ligands LXII-L_(Ai) that are based on a structure of Formula LXII

ligands LXIII-L_(Ai) that are based on a structure of Formula LXIII

ligands LXIV-L_(Ai) that are based on a structure of Formula LXIV

ligands LXV-L_(Ai) that are based on a structure of Formula LXV

wherein i is an integer from 1171 to 1584 and for each i, R¹, R¹¹, andR¹² in the formulas XVIII through XLIV and Formulas LXII, LXIII, LXIV,and LXV are defined as follows:

L_(Ai) R¹ R¹¹ R¹² L_(Ai) R¹ R¹¹ R¹² L_(Ai) R¹ R¹¹ R¹² L_(A1171) R_(B3) HH L_(A1309) R_(B7) H H L_(A1447) R_(B15) H H L_(A1172) R_(B3) R_(B1) HL_(A1310) R_(B7) R_(B1) H L_(A1448) R_(B15) R_(B1) H L_(A1173) R_(B3)R_(B3) H L_(A1311) R_(B7) R_(B3) H L_(A1449) R_(B15) R_(B3) H L_(A1174)R_(B3) R_(B4) H L_(A1312) R_(B7) R_(B4) H L_(A1450) R_(B15) R_(B4) HL_(A1175) R_(B3) R_(B5) H L_(A1313) R_(B7) R_(B5) H L_(A1451) R_(B15)R_(B5) H L_(A1176) R_(B3) R_(B6) H L_(A1314) R_(B7) R_(B6) H L_(A1452)R_(B15) R_(B6) H L_(A1177) R_(B3) R_(B7) H L_(A1315) R_(B7) R_(B7) HL_(A1453) R_(B15) R_(B7) H L_(A1178) R_(B3) R_(B24) H L_(A1316) R_(B7)R_(B24) H L_(A1454) R_(B15) R_(B24) H L_(A1179) R_(B3) R_(B25) HL_(A1317) R_(B7) R_(B25) H L_(A1455) R_(B15) R_(B25) H L_(A1180) R_(B3)R_(A3) H L_(A1318) R_(B7) R_(A3) H L_(A1456) R_(B15) R_(A3) H L_(A1181)R_(B3) R_(A34) H L_(A1319) R_(B7) R_(A34) H L_(A1457) R_(B15) R_(A34) HL_(A1182) R_(B3) R_(A44) H L_(A1320) R_(B7) R_(A44) H L_(A1458) R_(B15)R_(A44) H L_(A1183) R_(B3) R_(A52) H L_(A1321) R_(B7) R_(A52) HL_(A1459) R_(B15) R_(A52) H L_(A1184) R_(B3) R_(A53) H L_(A1322) R_(B7)R_(A53) H L_(A1460) R_(B15) R_(A53) H L_(A1185) R_(B3) R_(A54) HL_(A1323) R_(B7) R_(A54) H L_(A1461) R_(B15) R_(A54) H L_(A1186) R_(B3)R_(C3) H L_(A1324) R_(B7) R_(C3) H L_(A1462) R_(B15) R_(C3) H L_(A1187)R_(B3) R_(C4) H L_(A1325) R_(B7) R_(C4) H L_(A1463) R_(B15) R_(C4) HL_(A1188) R_(B3) R_(C8) H L_(A1326) R_(B7) R_(C8) H L_(A1464) R_(B15)R_(C8) H L_(A1189) R_(B3) H R_(B1) L_(A1327) R_(B7) H R_(B1) L_(A1465)R_(B15) H R_(B1) L_(A1190) R_(B3) H R_(B3) L_(A1328) R_(B7) H R_(B3)L_(A1466) R_(B15) H R_(B3) L_(A1191) R_(B3) H R_(B4) L_(A1329) R_(B7) HR_(B4) L_(A1467) R_(B15) H R_(B4) L_(A1192) R_(B3) H R_(B5) L_(A1330)R_(B7) H R_(B5) L_(A1468) R_(B15) H R_(B5) L_(A1193) R_(B3) H R_(B6)L_(A1331) R_(B7) H R_(B6) L_(A1469) R_(B15) H R_(B6) L_(A1194) R_(B3) HR_(B7) L_(A1332) R_(B7) H R_(B7) L_(A1470) R_(B15) H R_(B7) L_(A1195)R_(B3) H R_(B24) L_(A1333) R_(B7) H R_(B24) L_(A1471) R_(B15) H R_(B24)L_(A1196) R_(B3) H R_(B25) L_(A1334) R_(B7) H R_(B25) L_(A1472) R_(B15)H R_(B25) L_(A1197) R_(B3) H R_(A3) L_(A1335) R_(B7) H R_(A3) L_(A1473)R_(B15) H R_(A3) L_(A1198) R_(B3) H R_(A34) L_(A1336) R_(B7) H R_(A34)L_(A1474) R_(B15) H R_(A34) L_(A1199) R_(B3) H R_(A44) L_(A1337) R_(B7)H R_(A44) L_(A1475) R_(B15) H R_(A44) L_(A1200) R_(B3) H R_(A52)L_(A1338) R_(B7) H R_(A52) L_(A1476) R_(B15) H R_(A52) L_(A1201) R_(B3)H R_(A53) L_(A1339) R_(B7) H R_(A53) L_(A1477) R_(B15) H R_(A53)L_(A1202) R_(B3) H R_(A54) L_(A1340) R_(B7) H R_(A54) L_(A1478) R_(B15)H R_(A54) L_(A1203) R_(B3) H R_(C3) L_(A1341) R_(B7) H R_(C3) L_(A1479)R_(B15) H R_(C3) L_(A1204) R_(B3) H R_(C4) L_(A1342) R_(B7) H R_(C4)L_(A1480) R_(B15) H R_(C4) L_(A1205) R_(B3) H R_(C8) L_(A1343) R_(B7) HR_(C8) L_(A1481) R_(B15) H R_(C8) L_(A1206) R_(B3) R_(B1) R_(B1)L_(A1344) R_(B7) R_(B1) R_(B1) L_(A1482) R_(B15) R_(B1) R_(B1) L_(A1207)R_(B3) R_(B3) R_(B1) L_(A1345) R_(B7) R_(B3) R_(B1) L_(A1483) R_(B15)R_(B3) R_(B1) L_(A1208) R_(B3) R_(B4) R_(B1) L_(A1346) R_(B7) R_(B4)R_(B1) L_(A1484) R_(B15) R_(B4) R_(B1) L_(A1209) R_(B3) R_(B5) R_(B1)L_(A1347) R_(B7) R_(B5) R_(B1) L_(A1485) R_(B15) R_(B5) R_(B1) L_(A1210)R_(B3) R_(B6) R_(B1) L_(A1348) R_(B7) R_(B6) R_(B1) L_(A1486) R_(B15)R_(B6) R_(B1) L_(A1211) R_(B3) R_(B7) R_(B1) L_(A1349) R_(B7) R_(B7)R_(B1) L_(A1487) R_(B15) R_(B7) R_(B1) L_(A1212) R_(B3) R_(B24) R_(B1)L_(A1350) R_(B7) R_(B24) R_(B1) L_(A1488) R_(B15) R_(B24) R_(B1)L_(A1213) R_(B3) R_(B25) R_(B1) L_(A1351) R_(B7) R_(B25) R_(B1)L_(A1489) R_(B15) R_(B25) R_(B1) L_(A1214) R_(B3) R_(A3) R_(B1)L_(A1352) R_(B7) R_(A3) R_(B1) L_(A1490) R_(B15) R_(A3) R_(B1) L_(A1215)R_(B3) R_(A34) R_(B1) L_(A1353) R_(B7) R_(A34) R_(B1) L_(A1491) R_(B15)R_(A34) R_(B1) L_(A1216) R_(B3) R_(A44) R_(B1) L_(A1354) R_(B7) R_(A44)R_(B1) L_(A1492) R_(B15) R_(A44) R_(B1) L_(A1217) R_(B3) R_(A52) R_(B1)L_(A1355) R_(B7) R_(A52) R_(B1) L_(A1493) R_(B15) R_(A52) R_(B1)L_(A1218) R_(B3) R_(A53) R_(B1) L_(A1356) R_(B7) R_(A53) R_(B1)L_(A1494) R_(B15) R_(A53) R_(B1) L_(A1219) R_(B3) R_(A54) R_(B1)L_(A1357) R_(B7) R_(A54) R_(B1) L_(A1495) R_(B15) R_(A54) R_(B1)L_(A1220) R_(B3) R_(C3) R_(B1) L_(A1358) R_(B7) R_(C3) R_(B1) L_(A1496)R_(B15) R_(C3) R_(B1) L_(A1221) R_(B3) R_(C4) R_(B1) L_(A1359) R_(B7)R_(C4) R_(B1) L_(A1497) R_(B15) R_(C4) R_(B1) L_(A1222) R_(B3) R_(C8)R_(B1) L_(A1360) R_(B7) R_(C8) R_(B1) L_(A1498) R_(B15) R_(C8) R_(B1)L_(A1223) R_(B3) R_(B1) R_(B1) L_(A1361) R_(B7) R_(B1) R_(B1) L_(A1499)R_(B15) R_(B1) R_(B1) L_(A1224) R_(B3) R_(B1) R_(B3) L_(A1362) R_(B7)R_(B1) R_(B3) L_(A1500) R_(B15) R_(B1) R_(B3) L_(A1225) R_(B3) R_(B1)R_(B4) L_(A1363) R_(B7) R_(B1) R_(B4) L_(A1501) R_(B15) R_(B1) R_(B4)L_(A1226) R_(B3) R_(B1) R_(B5) L_(A1364) R_(B7) R_(B1) R_(B5) L_(A1502)R_(B15) R_(B1) R_(B5) L_(A1227) R_(B3) R_(B1) R_(B6) L_(A1365) R_(B7)R_(B1) R_(B6) L_(A1503) R_(B15) R_(B1) R_(B6) L_(A1228) R_(B3) R_(B1)R_(B7) L_(A1366) R_(B7) R_(B1) R_(B7) L_(A1504) R_(B15) R_(B1) R_(B7)L_(A1229) R_(B3) R_(B1) R_(B24) L_(A1367) R_(B7) R_(B1) R_(B24)L_(A1505) R_(B15) R_(B1) R_(B24) L_(A1230) R_(B3) R_(B1) R_(B25)L_(A1368) R_(B7) R_(B1) R_(B25) L_(A1506) R_(B15) R_(B1) R_(B25)L_(A1231) R_(B3) R_(B1) R_(A3) L_(A1369) R_(B7) R_(B1) R_(A3) L_(A1507)R_(B15) R_(B1) R_(A3) L_(A1232) R_(B3) R_(B1) R_(A34) L_(A1370) R_(B7)R_(B1) R_(A34) L_(A1508) R_(B15) R_(B1) R_(A34) L_(A1233) R_(B3) R_(B1)R_(A44) L_(A1371) R_(B7) R_(B1) R_(A44) L_(A1509) R_(B15) R_(B1) R_(A44)L_(A1234) R_(B3) R_(B1) R_(A52) L_(A1372) R_(B7) R_(B1) R_(A52)L_(A1510) R_(B15) R_(B1) R_(A52) L_(A1235) R_(B3) R_(B1) R_(A53)L_(A1373) R_(B7) R_(B1) R_(A53) L_(A1511) R_(B15) R_(B1) R_(A53)L_(A1236) R_(B3) R_(B1) R_(A54) L_(A1374) R_(B7) R_(B1) R_(A54)L_(A1512) R_(B15) R_(B1) R_(A54) L_(A1237) R_(B3) R_(B1) R_(C3)L_(A1375) R_(B7) R_(B1) R_(C3) L_(A1513) R_(B15) R_(B1) R_(C3) L_(A1238)R_(B3) R_(B1) R_(C4) L_(A1376) R_(B7) R_(B1) R_(C4) L_(A1514) R_(B15)R_(B1) R_(C4) L_(A1239) R_(B3) R_(B1) R_(C8) L_(A1377) R_(B7) R_(B1)R_(C8) L_(A1515) R_(B15) R_(B1) R_(C8) L_(A1240) R_(B6) H H L_(A1378)R_(B9) H H L_(A1516) R_(A44) H H L_(A1241) R_(B6) R_(B1) H L_(A1379)R_(B9) R_(B1) H L_(A1517) R_(A44) R_(B1) H L_(A1242) R_(B6) R_(B3) HL_(A1380) R_(B9) R_(B3) H L_(A1518) R_(A44) R_(B3) H L_(A1243) R_(B6)R_(B4) H L_(A1381) R_(B9) R_(B4) H L_(A1519) R_(A44) R_(B4) H L_(A1244)R_(B6) R_(B5) H L_(A1382) R_(B9) R_(B5) H L_(A1520) R_(A44) R_(B5) HL_(A1245) R_(B6) R_(B6) H L_(A1383) R_(B9) R_(B6) H L_(A1521) R_(A44)R_(B6) H L_(A1246) R_(B6) R_(B7) H L_(A1384) R_(B9) R_(B7) H L_(A1522)R_(A44) R_(B7) H L_(A1247) R_(B6) R_(B24) H L_(A1385) R_(B9) R_(B24) HL_(A1523) R_(A44) R_(B24) H L_(A1248) R_(B6) R_(B25) H L_(A1386) R_(B9)R_(B25) H L_(A1524) R_(A44) R_(B25) H L_(A1249) R_(B6) R_(A3) HL_(A1387) R_(B9) R_(A3) H L_(A1525) R_(A44) R_(A3) H L_(A1250) R_(B6)R_(A34) H L_(A1388) R_(B9) R_(A34) H L_(A1526) R_(A44) R_(A34) HL_(A1251) R_(B6) R_(A44) H L_(A1389) R_(B9) R_(A44) H L_(A1527) R_(A44)R_(A44) H L_(A1252) R_(B6) R_(A52) H L_(A1390) R_(B9) R_(A52) HL_(A1528) R_(A44) R_(A52) H L_(A1253) R_(B6) R_(A53) H L_(A1391) R_(B9)R_(A53) H L_(A1529) R_(A44) R_(A53) H L_(A1254) R_(B6) R_(A54) HL_(A1392) R_(B9) R_(A54) H L_(A1530) R_(A44) R_(A54) H L_(A1255) R_(B6)R_(C3) H L_(A1393) R_(B9) R_(C3) H L_(A1531) R_(A44) R_(C3) H L_(A1256)R_(B6) R_(C4) H L_(A1394) R_(B9) R_(C4) H L_(A1532) R_(A44) R_(C4) HL_(A1257) R_(B6) R_(C8) H L_(A1395) R_(B9) R_(C8) H L_(A1533) R_(A44)R_(C8) H L_(A1258) R_(B6) H R_(B1) L_(A1396) R_(B9) H R_(B1) L_(A1534)R_(A44) H R_(B1) L_(A1259) R_(B6) H R_(B3) L_(A1397) R_(B9) H R_(B3)L_(A1535) R_(A44) H R_(B3) L_(A1260) R_(B6) H R_(B4) L_(A1398) R_(B9) HR_(B4) L_(A1536) R_(A44) H R_(B4) L_(A1261) R_(B6) H R_(B5) L_(A1399)R_(B9) H R_(B5) L_(A1537) R_(A44) H R_(B5) L_(A1262) R_(B6) H R_(B6)L_(A1400) R_(B9) H R_(B6) L_(A1538) R_(A44) H R_(B6) L_(A1263) R_(B6) HR_(B7) L_(A1401) R_(B9) H R_(B7) L_(A1539) R_(A44) H R_(B7) L_(A1264)R_(B6) H R_(B24) L_(A1402) R_(B9) H R_(B24) L_(A1540) R_(A44) H R_(B24)L_(A1265) R_(B6) H R_(B25) L_(A1403) R_(B9) H R_(B25) L_(A1541) R_(A44)H R_(B25) L_(A1266) R_(B6) H R_(A3) L_(A1404) R_(B9) H R_(A3) L_(A1542)R_(A44) H R_(A3) L_(A1267) R_(B6) H R_(A34) L_(A1405) R_(B9) H R_(A34)L_(A1543) R_(A44) H R_(A34) L_(A1268) R_(B6) H R_(A44) L_(A1406) R_(B9)H R_(A44) L_(A1544) R_(A44) H R_(A44) L_(A1269) R_(B6) H R_(A52)L_(A1407) R_(B9) H R_(A52) L_(A1545) R_(A44) H R_(A52) L_(A1270) R_(B6)H R_(A53) L_(A1408) R_(B9) H R_(A53) L_(A1546) R_(A44) H R_(A53)L_(A1271) R_(B6) H R_(A54) L_(A1409) R_(B9) H R_(A54) L_(A1547) R_(A44)H R_(A54) L_(A1272) R_(B6) H R_(C3) L_(A1410) R_(B9) H R_(C3) L_(A1548)R_(A44) H R_(C3) L_(A1273) R_(B6) H R_(C4) L_(A1411) R_(B9) H R_(C4)L_(A1549) R_(A44) H R_(C4) L_(A1274) R_(B6) H R_(C8) L_(A1412) R_(B9) HR_(C8) L_(A1550) R_(A44) H R_(C8) L_(A1275) R_(B6) R_(B1) R_(B1)L_(A1413) R_(B9) R_(B1) R_(B1) L_(A1551) R_(A44) R_(B1) R_(B1) L_(A1276)R_(B6) R_(B3) R_(B1) L_(A1414) R_(B9) R_(B3) R_(B1) L_(A1552) R_(A44)R_(B3) R_(B1) L_(A1277) R_(B6) R_(B4) R_(B1) L_(A1415) R_(B9) R_(B4)R_(B1) L_(A1553) R_(A44) R_(B4) R_(B1) L_(A1278) R_(B6) R_(B5) R_(B1)L_(A1416) R_(B9) R_(B5) R_(B1) L_(A1554) R_(A44) R_(B5) R_(B1) L_(A1279)R_(B6) R_(B6) R_(B1) L_(A1417) R_(B9) R_(B6) R_(B1) L_(A1555) R_(A44)R_(B6) R_(B1) L_(A1280) R_(B6) R_(B7) R_(B1) L_(A1418) R_(B9) R_(B7)R_(B1) L_(A1556) R_(A44) R_(B7) R_(B1) L_(A1281) R_(B6) R_(B24) R_(B1)L_(A1419) R_(B9) R_(B24) R_(B1) L_(A1557) R_(A44) R_(B24) R_(B1)L_(A1282) R_(B6) R_(B25) R_(B1) L_(A1420) R_(B9) R_(B25) R_(B1)L_(A1558) R_(A44) R_(B25) R_(B1) L_(A1283) R_(B6) R_(A3) R_(B1)L_(A1421) R_(B9) R_(A3) R_(B1) L_(A1559) R_(A44) R_(A3) R_(B1) L_(A1284)R_(B6) R_(A34) R_(B1) L_(A1422) R_(B9) R_(A34) R_(B1) L_(A1560) R_(A44)R_(A34) R_(B1) L_(A1285) R_(B6) R_(A44) R_(B1) L_(A1423) R_(B9) R_(A44)R_(B1) L_(A1561) R_(A44) R_(A44) R_(B1) L_(A1286) R_(B6) R_(A52) R_(B1)L_(A1424) R_(B9) R_(A52) R_(B1) L_(A1562) R_(A44) R_(A52) R_(B1)L_(A1287) R_(B6) R_(A53) R_(B1) L_(A1425) R_(B9) R_(A53) R_(B1)L_(A1563) R_(A44) R_(A53) R_(B1) L_(A1288) R_(B6) R_(A54) R_(B1)L_(A1426) R_(B9) R_(A54) R_(B1) L_(A1564) R_(A44) R_(A54) R_(B1)L_(A1289) R_(B6) R_(C3) R_(B1) L_(A1427) R_(B9) R_(C3) R_(B1) L_(A1565)R_(A44) R_(C3) R_(B1) L_(A1290) R_(B6) R_(C4) R_(B1) L_(A1428) R_(B9)R_(C4) R_(B1) L_(A1566) R_(A44) R_(C4) R_(B1) L_(A1291) R_(B6) R_(C8)R_(B1) L_(A1429) R_(B9) R_(C8) R_(B1) L_(A1567) R_(A44) R_(C8) R_(B1)L_(A1292) R_(B6) R_(B1) R_(B1) L_(A1430) R_(B9) R_(B1) R_(B1) L_(A1568)R_(A44) R_(B1) R_(B1) L_(A1293) R_(B6) R_(B1) R_(B3) L_(A1431) R_(B9)R_(B1) R_(B3) L_(A1569) R_(A44) R_(B1) R_(B3) L_(A1294) R_(B6) R_(B1)R_(B4) L_(A1432) R_(B9) R_(B1) R_(B4) L_(A1570) R_(A44) R_(B1) R_(B4)L_(A1295) R_(B6) R_(B1) R_(B5) L_(A1433) R_(B9) R_(B1) R_(B5) L_(A1571)R_(A44) R_(B1) R_(B5) L_(A1296) R_(B6) R_(B1) R_(B6) L_(A1434) R_(B9)R_(B1) R_(B6) L_(A1572) R_(A44) R_(B1) R_(B6) L_(A1297) R_(B6) R_(B1)R_(B7) L_(A1435) R_(B9) R_(B1) R_(B7) L_(A1573) R_(A44) R_(B1) R_(B7)L_(A1298) R_(B6) R_(B1) R_(B24) L_(A1436) R_(B9) R_(B1) R_(B24)L_(A1574) R_(A44) R_(B1) R_(B24) L_(A1299) R_(B6) R_(B1) R_(B25)L_(A1437) R_(B9) R_(B1) R_(B25) L_(A1575) R_(A44) R_(B1) R_(B25)L_(A1300) R_(B6) R_(B1) R_(A3) L_(A1438) R_(B9) R_(B1) R_(A3) L_(A1576)R_(A44) R_(B1) R_(A3) L_(A1301) R_(B6) R_(B1) R_(A34) L_(A1439) R_(B9)R_(B1) R_(A34) L_(A1577) R_(A44) R_(B1) R_(A34) L_(A1302) R_(B6) R_(B1)R_(A44) L_(A1440) R_(B9) R_(B1) R_(A44) L_(A1578) R_(A44) R_(B1) R_(A44)L_(A1303) R_(B6) R_(B1) R_(A52) L_(A1441) R_(B9) R_(B1) R_(A52)L_(A1579) R_(A44) R_(B1) R_(A52) L_(A1304) R_(B6) R_(B1) R_(A53)L_(A1442) R_(B9) R_(B1) R_(A53) L_(A1580) R_(A44) R_(B1) R_(A53)L_(A1305) R_(B6) R_(B1) R_(A54) L_(A1443) R_(B9) R_(B1) R_(A54)L_(A1581) R_(A44) R_(B1) R_(A54) L_(A1306) R_(B6) R_(B1) R_(C3)L_(A1444) R_(B9) R_(B1) R_(C3) L_(A1582) R_(A44) R_(B1) R_(C3) L_(A1307)R_(B6) R_(B1) R_(C4) L_(A1445) R_(B9) R_(B1) R_(C4) L_(A1583) R_(A44)R_(B1) R_(C4) L_(A1308) R_(B6) R_(B1) R_(C8) L_(A1446) R_(B9) R_(B1)R_(C8) L_(A1584) R_(A44) R_(B1) R_(C8)

In some embodiments of Formula IA, the first ligand L_(A) is selectedfrom the group consisting of:

ligands XLV-L_(Ai) that are based on a structure of Formula XLV

ligands XLVI-L_(Ai) that are based on a structure of Formula XLVI

ligands XLVII-L_(Ai) that are based on a structure of Formula XLVII

ligands XLVIII-L_(Ai) that are based on a structure of Formula XLVIII

ligands XLIX-L_(Ai) that are based on a structure of Formula XLIX

ligands L-L_(Ai) that are based on a structure of Formula LI

wherein i is an integer from 1585 to 1970 and for each i, R¹, R², R¹¹,and R¹² in the formulas XLV through LI are defined as follows:

L_(Ai) R¹ R¹¹ R¹² R² L_(Ai) R¹ R¹¹ R¹² R² L_(A1585) H H H R_(B1)L_(A1778) H H H R_(A54) L_(A1586) H R_(B1) H R_(B1) L_(A1779) H R_(B1) HR_(A54) L_(A1587) H R_(B3) H R_(B1) L_(A1780) H R_(B3) H R_(A54)L_(A1588) H R_(B4) H R_(B1) L_(A1781) H R_(B4) H R_(A54) L_(A1589) HR_(B5) H R_(B1) L_(A1782) H R_(B5) H R_(A54) L_(A1590) H R_(B6) H R_(B1)L_(A1783) H R_(B6) H R_(A54) L_(A1591) H R_(B7) H R_(B1) L_(A1784) HR_(B7) H R_(A54) L_(A1592) H R_(B24) H R_(B1) L_(A1785) H R_(B24) HR_(A54) L_(A1593) H R_(B25) H R_(B1) L_(A1786) H R_(B25) H R_(A54)L_(A1594) H R_(A3) H R_(B1) L_(A1787) H R_(A3) H R_(A54) L_(A1595) HR_(A34) H R_(B1) L_(A1788) H R_(A34) H R_(A54) L_(A1596) H R_(A44) HR_(B1) L_(A1789) H R_(A44) H R_(A54) L_(A1597) H R_(A52) H R_(B1)L_(A1790) H R_(A52) H R_(A54) L_(A1598) H R_(A53) H R_(B1) L_(A1791) HR_(A53) H R_(A54) L_(A1599) H R_(A54) H R_(B1) L_(A1792) H R_(A54) HR_(A54) L_(A1600) H R_(C3) H R_(B1) L_(A1793) H R_(C3) H R_(A54)L_(A1601) H R_(C4) H R_(B1) L_(A1794) H R_(C4) H R_(A54) L_(A1602) HR_(C8) H R_(B1) L_(A1795) H R_(C8) H R_(A54) L_(A1603) H H R_(B1) R_(B1)L_(A1796) H H R_(B1) R_(A54) L_(A1604) H H R_(B3) R_(B1) L_(A1797) H HR_(B3) R_(A54) L_(A1605) H H R_(B4) R_(B1) L_(A1798) H H R_(B4) R_(A54)L_(A1606) H H R_(B5) R_(B1) L_(A1799) H H R_(B5) R_(A54) L_(A1607) H HR_(B6) R_(B1) L_(A1800) H H R_(B6) R_(A54) L_(A1608) H H R_(B7) R_(B1)L_(A1801) H H R_(B7) R_(A54) L_(A1609) H H R_(B24) R_(B1) L_(A1802) H HR_(B24) R_(A54) L_(A1610) H H R_(B25) R_(B1) L_(A1803) H H R_(B25)R_(A54) L_(A1611) H H R_(A3) R_(B1) L_(A1804) H H R_(A3) R_(A54)L_(A1612) H H R_(A34) R_(B1) L_(A1805) H H R_(A34) R_(A54) L_(A1613) H HR_(A44) R_(B1) L_(A1806) H H R_(A44) R_(A54) L_(A1614) H H R_(A52)R_(B1) L_(A1807) H H R_(A52) R_(A54) L_(A1615) H H R_(A53) R_(B1)L_(A1808) H H R_(A53) R_(A54) L_(A1616) H H R_(A54) R_(B1) L_(A1809) H HR_(A54) R_(A54) L_(A1617) H H R_(C3) R_(B1) L_(A1810) H H R_(C3) R_(A54)L_(A1618) H H R_(C4) R_(B1) L_(A1811) H H R_(C4) R_(A54) L_(A1619) H HR_(C8) R_(B1) L_(A1812) H H R_(C8) R_(A54) L_(A1620) H R_(B1) R_(B1)R_(B1) L_(A1813) H R_(B1) R_(B1) R_(A54) L_(A1621) H R_(B3) R_(B1)R_(B1) L_(A1814) H R_(B3) R_(B1) R_(A54) L_(A1622) H R_(B4) R_(B1)R_(B1) L_(A1815) H R_(B4) R_(B1) R_(A54) L_(A1623) H R_(B5) R_(B1)R_(B1) L_(A1816) H R_(B5) R_(B1) R_(A54) L_(A1624) H R_(B6) R_(B1)R_(B1) L_(A1817) H R_(B6) R_(B1) R_(A54) L_(A1625) H R_(B7) R_(B1)R_(B1) L_(A1818) H R_(B7) R_(B1) R_(A54) L_(A1626) H R_(B24) R_(B1)R_(B1) L_(A1819) H R_(B24) R_(B1) R_(A54) L_(A1627) H R_(B25) R_(B1)R_(B1) L_(A1820) H R_(B25) R_(B1) R_(A54) L_(A1628) H R_(A3) R_(B1)R_(B1) L_(A1821) H R_(A3) R_(B1) R_(A54) L_(A1629) H R_(A34) R_(B1)R_(B1) L_(A1822) H R_(A34) R_(B1) R_(A54) L_(A1630) H R_(A44) R_(B1)R_(B1) L_(A1823) H R_(A44) R_(B1) R_(A54) L_(A1631) H R_(A52) R_(B1)R_(B1) L_(A1824) H R_(A52) R_(B1) R_(A54) L_(A1632) H R_(A53) R_(B1)R_(B1) L_(A1825) H R_(A53) R_(B1) R_(A54) L_(A1633) H R_(A54) R_(B1)R_(B1) L_(A1826) H R_(A54) R_(B1) R_(A54) L_(A1634) H R_(C3) R_(B1)R_(B1) L_(A1827) H R_(C3) R_(B1) R_(A54) L_(A1635) H R_(C4) R_(B1)R_(B1) L_(A1828) H R_(C4) R_(B1) R_(A54) L_(A1636) H R_(C8) R_(B1)R_(B1) L_(A1829) H R_(C8) R_(B1) R_(A54) L_(A1637) H R_(B1) R_(B1)R_(B1) L_(A1830) H R_(B1) R_(B1) R_(A54) L_(A1638) H R_(B1) R_(B3)R_(B1) L_(A1831) H R_(B1) R_(B3) R_(A54) L_(A1639) H R_(B1) R_(B4)R_(B1) L_(A1832) H R_(B1) R_(B4) R_(A54) L_(A1640) H R_(B1) R_(B5)R_(B1) L_(A1833) H R_(B1) R_(B5) R_(A54) L_(A1641) H R_(B1) R_(B6)R_(B1) L_(A1834) H R_(B1) R_(B6) R_(A54) L_(A1642) H R_(B1) R_(B7)R_(B1) L_(A1835) H R_(B1) R_(B7) R_(A54) L_(A1643) H R_(B1) R_(B24)R_(B1) L_(A1836) H R_(B1) R_(B24) R_(A54) L_(A1644) H R_(B1) R_(B25)R_(B1) L_(A1837) H R_(B1) R_(B25) R_(A54) L_(A1645) H R_(B1) R_(A3)R_(B1) L_(A1838) H R_(B1) R_(A3) R_(A54) L_(A1646) H R_(B1) R_(A34)R_(B1) L_(A1839) H R_(B1) R_(A34) R_(A54) L_(A1647) H R_(B1) R_(A44)R_(B1) L_(A1840) H R_(B1) R_(A44) R_(A54) L_(A1648) H R_(B1) R_(A52)R_(B1) L_(A1841) H R_(B1) R_(A52) R_(A54) L_(A1649) H R_(B1) R_(A53)R_(B1) L_(A1842) H R_(B1) R_(A53) R_(A54) L_(A1650) H R_(B1) R_(A54)R_(B1) L_(A1843) H R_(B1) R_(A54) R_(A54) L_(A1651) H R_(B1) R_(C3)R_(B1) L_(A1844) H R_(B1) R_(C3) R_(A54) L_(A1652) H R_(B1) R_(C4)R_(B1) L_(A1845) H R_(B1) R_(C4) R_(A54) L_(A1653) H R_(B1) R_(C8)R_(B1) L_(A1846) H R_(B1) R_(C8) R_(A54) L_(A1654) R_(B1) H H R_(B1)L_(A1847) R_(B1) H H R_(A54) L_(A1655) R_(B1) R_(B1) H R_(B1) L_(A1848)R_(B1) R_(B1) H R_(A54) L_(A1656) R_(B1) R_(B3) H R_(B1) L_(A1849)R_(B1) R_(B3) H R_(A54) L_(A1657) R_(B1) R_(B4) H R_(B1) L_(A1850)R_(B1) R_(B4) H R_(A54) L_(A1658) R_(B1) R_(B5) H R_(B1) L_(A1851)R_(B1) R_(B5) H R_(A54) L_(A1659) R_(B1) R_(B6) H R_(B1) L_(A1852)R_(B1) R_(B6) H R_(A54) L_(A1660) R_(B1) R_(B7) H R_(B1) L_(A1853)R_(B1) R_(B7) H R_(A54) L_(A1661) R_(B1) R_(B24) H R_(B1) L_(A1854)R_(B1) R_(B24) H R_(A54) L_(A1662) R_(B1) R_(B25) H R_(B1) L_(A1855)R_(B1) R_(B25) H R_(A54) L_(A1663) R_(B1) R_(A3) H R_(B1) L_(A1856)R_(B1) R_(A3) H R_(A54) L_(A1664) R_(B1) R_(A34) H R_(B1) L_(A1857)R_(B1) R_(A34) H R_(A54) L_(A1665) R_(B1) R_(A44) H R_(B1) L_(A1858)R_(B1) R_(A44) H R_(A54) L_(A1666) R_(B1) R_(A52) H R_(B1) L_(A1859)R_(B1) R_(A52) H R_(A54) L_(A1667) R_(B1) R_(A53) H R_(B1) L_(A1860)R_(B1) R_(A53) H R_(A54) L_(A1668) R_(B1) R_(A54) H R_(B1) L_(A1861)R_(B1) R_(A54) H R_(A54) L_(A1669) R_(B1) R_(C3) H R_(B1) L_(A1862)R_(B1) R_(C3) H R_(A54) L_(A1670) R_(B1) R_(C4) H R_(B1) L_(A1863)R_(B1) R_(C4) H R_(A54) L_(A1671) R_(B1) R_(C8) H R_(B1) L_(A1864)R_(B1) R_(C8) H R_(A54) L_(A1672) R_(B1) H R_(B1) R_(B1) L_(A1865)R_(B1) H R_(B1) R_(A54) L_(A1673) R_(B1) H R_(B3) R_(B1) L_(A1866)R_(B1) H R_(B3) R_(A54) L_(A1674) R_(B1) H R_(B4) R_(B1) L_(A1867)R_(B1) H R_(B4) R_(A54) L_(A1675) R_(B1) H R_(B5) R_(B1) L_(A1868)R_(B1) H R_(B5) R_(A54) L_(A1676) R_(B1) H R_(B6) R_(B1) L_(A1869)R_(B1) H R_(B6) R_(A54) L_(A1677) R_(B1) H R_(B7) R_(B1) L_(A1870)R_(B1) H R_(B7) R_(A54) L_(A1678) R_(B1) H R_(B24) R_(B1) L_(A1871)R_(B1) H R_(B24) R_(A54) L_(A1679) R_(B1) H R_(B25) R_(B1) L_(A1872)R_(B1) H R_(B25) R_(A54) L_(A1680) R_(B1) H R_(A3) R_(B1) L_(A1873)R_(B1) H R_(A3) R_(A54) L_(A1681) R_(B1) H R_(A34) R_(B1) L_(A1874)R_(B1) H R_(A34) R_(A54) L_(A1682) R_(B1) H R_(A44) R_(B1) L_(A1875)R_(B1) H R_(A44) R_(A54) L_(A1683) R_(B1) H R_(A52) R_(B1) L_(A1876)R_(B1) H R_(A52) R_(A54) L_(A1684) R_(B1) H R_(A53) R_(B1) L_(A1877)R_(B1) H R_(A53) R_(A54) L_(A1685) R_(B1) H R_(A54) R_(B1) L_(A1878)R_(B1) H R_(A54) R_(A54) L_(A1686) R_(B1) H R_(C3) R_(B1) L_(A1879)R_(B1) H R_(C3) R_(A54) L_(A1687) R_(B1) H R_(C4) R_(B1) L_(A1880)R_(B1) H R_(C4) R_(A54) L_(A1688) R_(B1) H R_(C8) R_(B1) L_(A1881)R_(B1) H R_(C8) R_(A54) L_(A1689) R_(B1) R_(B1) R_(B1) R_(B1) L_(A1882)R_(B1) R_(B1) R_(B1) R_(A54) L_(A1690) R_(B1) R_(B3) R_(B1) R_(B1)L_(A1883) R_(B1) R_(B3) R_(B1) R_(A54) L_(A1691) R_(B1) R_(B4) R_(B1)R_(B1) L_(A1884) R_(B1) R_(B4) R_(B1) R_(A54) L_(A1692) R_(B1) R_(B5)R_(B1) R_(B1) L_(A1885) R_(B1) R_(B5) R_(B1) R_(A54) L_(A1693) R_(B1)R_(B6) R_(B1) R_(B1) L_(A1886) R_(B1) R_(B6) R_(B1) R_(A54) L_(A1694)R_(B1) R_(B7) R_(B1) R_(B1) L_(A1887) R_(B1) R_(B7) R_(B1) R_(A54)L_(A1695) R_(B1) R_(B24) R_(B1) R_(B1) L_(A1888) R_(B1) R_(B24) R_(B1)R_(A54) L_(A1696) R_(B1) R_(B25) R_(B1) R_(B1) L_(A1889) R_(B1) R_(B25)R_(B1) R_(A54) L_(A1697) R_(B1) R_(A3) R_(B1) R_(B1) L_(A1890) R_(B1)R_(A3) R_(B1) R_(A54) L_(A1698) R_(B1) R_(A34) R_(B1) R_(B1) L_(A1891)R_(B1) R_(A34) R_(B1) R_(A54) L_(A1699) R_(B1) R_(A44) R_(B1) R_(B1)L_(A1892) R_(B1) R_(A44) R_(B1) R_(A54) L_(A1700) R_(B1) R_(A52) R_(B1)R_(B1) L_(A1893) R_(B1) R_(A52) R_(B1) R_(A54) L_(A1701) R_(B1) R_(A53)R_(B1) R_(B1) L_(A1894) R_(B1) R_(A53) R_(B1) R_(A54) L_(A1702) R_(B1)R_(A54) R_(B1) R_(B1) L_(A1895) R_(B1) R_(A54) R_(B1) R_(A54) L_(A1703)R_(B1) R_(C3) R_(B1) R_(B1) L_(A1896) R_(B1) R_(C3) R_(B1) R_(A54)L_(A1704) R_(B1) R_(C4) R_(B1) R_(B1) L_(A1897) R_(B1) R_(C4) R_(B1)R_(A54) L_(A1705) R_(B1) R_(C8) R_(B1) R_(B1) L_(A1898) R_(B1) R_(C8)R_(B1) R_(A54) L_(A1706) R_(B1) R_(B1) R_(B1) R_(B1) L_(A1899) R_(B1)R_(B1) R_(B1) R_(A54) L_(A1707) R_(B1) R_(B1) R_(B3) R_(B1) L_(A1900)R_(B1) R_(B1) R_(B3) R_(A54) L_(A1708) R_(B1) R_(B1) R_(B4) R_(B1)L_(A1901) R_(B1) R_(B1) R_(B4) R_(A54) L_(A1709) R_(B1) R_(B1) R_(B5)R_(B1) L_(A1902) R_(B1) R_(B1) R_(B5) R_(A54) L_(A1710) R_(B1) R_(B1)R_(B6) R_(B1) L_(A1903) R_(B1) R_(B1) R_(B6) R_(A54) L_(A1711) R_(B1)R_(B1) R_(B7) R_(B1) L_(A1904) R_(B1) R_(B1) R_(B7) R_(A54) L_(A1712)R_(B1) R_(B1) R_(B24) R_(B1) L_(A1905) R_(B1) R_(B1) R_(B24) R_(A54)L_(A1713) R_(B1) R_(B1) R_(B25) R_(B1) L_(A1906) R_(B1) R_(B1) R_(B25)R_(A54) L_(A1714) R_(B1) R_(B1) R_(A3) R_(B1) L_(A1907) R_(B1) R_(B1)R_(A3) R_(A54) L_(A1715) R_(B1) R_(B1) R_(A34) R_(B1) L_(A1908) R_(B1)R_(B1) R_(A34) R_(A54) L_(A1716) R_(B6) H H R_(B1) L_(A1909) R_(B6) H HR_(A54) L_(A1717) R_(B6) R_(B1) H R_(B1) L_(A1910) R_(B6) R_(B1) HR_(A54) L_(A1718) R_(B6) R_(B3) H R_(B1) L_(A1911) R_(B6) R_(B3) HR_(A54) L_(A1719) R_(B6) R_(B4) H R_(B1) L_(A1912) R_(B6) R_(B4) HR_(A54) L_(A1720) R_(B6) R_(B5) H R_(B1) L_(A1913) R_(B6) R_(B5) HR_(A54) L_(A1721) R_(B6) R_(B6) H R_(B1) L_(A1914) R_(B6) R_(B6) HR_(A54) L_(A1722) R_(B6) R_(B7) H R_(B1) L_(A1915) R_(B6) R_(B7) HR_(A54) L_(A1723) R_(B6) R_(B24) H R_(B1) L_(A1916) R_(B6) R_(B24) HR_(A54) L_(A1724) R_(B6) R_(B25) H R_(B1) L_(A1917) R_(B6) R_(B25) HR_(A54) L_(A1725) R_(B6) R_(A3) H R_(B1) L_(A1918) R_(B6) R_(A3) HR_(A54) L_(A1726) R_(B6) R_(A34) H R_(B1) L_(A1919) R_(B6) R_(A34) HR_(A54) L_(A1727) R_(B6) R_(A44) H R_(B1) L_(A1920) R_(B6) R_(A44) HR_(A54) L_(A1728) R_(B6) R_(A52) H R_(B1) L_(A1921) R_(B6) R_(A52) HR_(A54) L_(A1729) R_(B6) R_(A53) H R_(B1) L_(A1922) R_(B6) R_(A53) HR_(A54) L_(A1730) R_(B6) R_(A54) H R_(B1) L_(A1923) R_(B6) R_(A54) HR_(A54) L_(A1731) R_(B6) R_(C3) H R_(B1) L_(A1924) R_(B6) R_(C3) HR_(A54) L_(A1732) R_(B6) R_(C4) H R_(B1) L_(A1925) R_(B6) R_(C4) HR_(A54) L_(A1733) R_(B6) R_(C8) H R_(B1) L_(A1926) R_(B6) R_(C8) HR_(A54) L_(A1734) R_(B6) H R_(B1) R_(B1) L_(A1927) R_(B6) H R_(B1)R_(A54) L_(A1735) R_(B6) H R_(B3) R_(B1) L_(A1928) R_(B6) H R_(B3)R_(A54) L_(A1736) R_(B6) H R_(B4) R_(B1) L_(A1929) R_(B6) H R_(B4)R_(A54) L_(A1737) R_(B6) H R_(B5) R_(B1) L_(A1930) R_(B6) H R_(B5)R_(A54) L_(A1738) R_(B6) H R_(B6) R_(B1) L_(A1931) R_(B6) H R_(B6)R_(A54) L_(A1739) R_(B6) H R_(B7) R_(B1) L_(A1932) R_(B6) H R_(B7)R_(A54) L_(A1740) R_(B6) H R_(B24) R_(B1) L_(A1933) R_(B6) H R_(B24)R_(A54) L_(A1741) R_(B6) H R_(B25) R_(B1) L_(A1934) R_(B6) H R_(B25)R_(A54) L_(A1742) R_(B6) H R_(A3) R_(B1) L_(A1935) R_(B6) H R_(A3)R_(A54) L_(A1743) R_(B6) H R_(A34) R_(B1) L_(A1936) R_(B6) H R_(A34)R_(A54) L_(A1744) R_(B6) H R_(A44) R_(B1) L_(A1937) R_(B6) H R_(A44)R_(A54) L_(A1745) R_(B6) H R_(A52) R_(B1) L_(A1938) R_(B6) H R_(A52)R_(A54) L_(A1746) R_(B6) H R_(A53) R_(B1) L_(A1939) R_(B6) H R_(A53)R_(A54) L_(A1747) R_(B6) H R_(A54) R_(B1) L_(A1940) R_(B6) H R_(A54)R_(A54) L_(A1748) R_(B6) H R_(C3) R_(B1) L_(A1941) R_(B6) H R_(C3)R_(A54) L_(A1749) R_(B6) H R_(C4) R_(B1) L_(A1942) R_(B6) H R_(C4)R_(A54) L_(A1750) R_(B6) H R_(C8) R_(B1) L_(A1943) R_(B6) H R_(C8)R_(A54) L_(A1751) R_(B6) R_(B1) R_(B1) R_(B1) L_(A1944) R_(B6) R_(B1)R_(B1) R_(A54) L_(A1752) R_(B6) R_(B3) R_(B1) R_(B1) L_(A1945) R_(B6)R_(B3) R_(B1) R_(A54) L_(A1753) R_(B6) R_(B4) R_(B1) R_(B1) L_(A1946)R_(B6) R_(B4) R_(B1) R_(A54) L_(A1754) R_(B6) R_(B5) R_(B1) R_(B1)L_(A1947) R_(B6) R_(B5) R_(B1) R_(A54) L_(A1755) R_(B6) R_(B6) R_(B1)R_(B1) L_(A1948) R_(B6) R_(B6) R_(B1) R_(A54) L_(A1756) R_(B6) R_(B7)R_(B1) R_(B1) L_(A1949) R_(B6) R_(B7) R_(B1) R_(A54) L_(A1757) R_(B6)R_(B24) R_(B1) R_(B1) L_(A1950) R_(B6) R_(B24) R_(B1) R_(A54) L_(A1758)R_(B6) R_(B25) R_(B1) R_(B1) L_(A1951) R_(B6) R_(B25) R_(B1) R_(A54)L_(A1759) R_(B6) R_(A3) R_(B1) R_(B1) L_(A1952) R_(B6) R_(A3) R_(B1)R_(A54) L_(A1760) R_(B6) R_(A34) R_(B1) R_(B1) L_(A1953) R_(B6) R_(A34)R_(B1) R_(A54) L_(A1761) R_(B6) R_(A44) R_(B1) R_(B1) L_(A1954) R_(B6)R_(A44) R_(B1) R_(A54) L_(A1762) R_(B6) R_(A52) R_(B1) R_(B1) L_(A1955)R_(B6) R_(A52) R_(B1) R_(A54) L_(A1763) R_(B6) R_(A53) R_(B1) R_(B1)L_(A1956) R_(B6) R_(A53) R_(B1) R_(A54) L_(A1764) R_(B6) R_(A54) R_(B1)R_(B1) L_(A1957) R_(B6) R_(A54) R_(B1) R_(A54) L_(A1765) R_(B6) R_(C3)R_(B1) R_(B1) L_(A1958) R_(B6) R_(C3) R_(B1) R_(A54) L_(A1766) R_(B6)R_(C4) R_(B1) R_(B1) L_(A1959) R_(B6) R_(C4) R_(B1) R_(A54) L_(A1767)R_(B6) R_(C8) R_(B1) R_(B1) L_(A1960) R_(B6) R_(C8) R_(B1) R_(A54)L_(A1768) R_(B6) R_(B1) R_(B1) R_(B1) L_(A1961) R_(B6) R_(B1) R_(B1)R_(A54) L_(A1769) R_(B6) R_(B1) R_(B3) R_(B1) L_(A1962) R_(B6) R_(B1)R_(B3) R_(A54) L_(A1770) R_(B6) R_(B1) R_(B4) R_(B1) L_(A1963) R_(B6)R_(B1) R_(B4) R_(A54) L_(A1771) R_(B6) R_(B1) R_(B5) R_(B1) L_(A1964)R_(B6) R_(B1) R_(B5) R_(A54) L_(A1772) R_(B6) R_(B1) R_(B6) R_(B1)L_(A1965) R_(B6) R_(B1) R_(B6) R_(A54) L_(A1773) R_(B6) R_(B1) R_(B7)R_(B1) L_(A1966) R_(B6) R_(B1) R_(B7) R_(A54) L_(A1774) R_(B6) R_(B1)R_(B24) R_(B1) L_(A1967) R_(B6) R_(B1) R_(B24) R_(A54) L_(A1775) R_(B6)R_(B1) R_(B25) R_(B1) L_(A1968) R_(B6) R_(B1) R_(B25) R_(A54) L_(A1776)R_(B6) R_(B1) R_(A3) R_(B1) L_(A1969) R_(B6) R_(B1) R_(A3) R_(A54)L_(A1777) R_(B6) R_(B1) R_(A34) R_(B1) L_(A1970) R_(B6) R_(B1) R_(A34)R_(A54)

In some embodiments of the compound, the first ligand L_(A) is selectedfrom the group consisting of

ligands LII-L_(Ai) that are based on a structure of Formula LII

ligands LIII-L_(Ai) that are based on a structure of Formula LIII

ligands LIV-L_(Ai) that are based on a structure of Formula LIN

ligands LV-L_(Ai) that are based on a structure of Formula LV

ligands LVI-L_(Ai) that are based on a structure of Formula LVI

wherein i is an integer from 1971 to 2186 and for each i, R¹, R², andR¹⁴ in the formulas LII through LVI are defined as follows:

L_(Ai) R¹ R¹⁴ R² L_(Ai) R¹ R¹⁴ R² L_(Ai) R¹ R¹⁴ R² L_(A1971) R_(B3) H HL_(A2043) R_(B15) H H L_(A2115) H H R_(A54) L_(A1972) R_(B3) R_(B1) HL_(A2044) R_(B15) R_(B1) H L_(A2116) H R_(B1) R_(A54) L_(A1973) R_(B3)R_(B3) H L_(A2045) R_(B15) R_(B3) H L_(A2117) H R_(B3) R_(A54) L_(A1974)R_(B3) R_(B4) H L_(A2046) R_(B15) R_(B4) H L_(A2118) H R_(B4) R_(A54)L_(A1975) R_(B3) R_(B5) H L_(A2047) R_(B15) R_(B5) H L_(A2119) H R_(B5)R_(A54) L_(A1976) R_(B3) R_(B6) H L_(A2048) R_(B15) R_(B6) H L_(A2120) HR_(B6) R_(A54) L_(A1977) R_(B3) R_(B7) H L_(A2049) R_(B15) R_(B7) HL_(A2121) H R_(B7) R_(A54) L_(A1978) R_(B3) R_(B24) H L_(A2050) R_(B15)R_(B24) H L_(A2122) H R_(B24) R_(A54) L_(A1979) R_(B3) R_(B25) HL_(A2051) R_(B15) R_(B25) H L_(A2123) H R_(B25) R_(A54) L_(A1980) R_(B3)R_(A3) H L_(A2052) R_(B15) R_(A3) H L_(A2124) H R_(A3) R_(A54) L_(A1981)R_(B3) R_(A34) H L_(A2053) R_(B15) R_(A34) H L_(A2125) H R_(A34) R_(A54)L_(A1982) R_(B3) R_(A44) H L_(A2054) R_(B15) R_(A44) H L_(A2126) HR_(A44) R_(A54) L_(A1983) R_(B3) R_(A52) H L_(A2055) R_(B15) R_(A52) HL_(A2127) H R_(A52) R_(A54) L_(A1984) R_(B3) R_(A53) H L_(A2056) R_(B15)R_(A53) H L_(A2128) H R_(A53) R_(A54) L_(A1985) R_(B3) R_(A54) HL_(A2057) R_(B15) R_(A54) H L_(A2129) H R_(A54) R_(A54) L_(A1986) R_(B3)R_(C3) H L_(A2058) R_(B15) R_(C3) H L_(A2130) H R_(C3) R_(A54) L_(A1987)R_(B3) R_(C4) H L_(A2059) R_(B15) R_(C4) H L_(A2131) H R_(C4) R_(A54)L_(A1988) R_(B3) R_(C8) H L_(A2060) R_(B15) R_(C8) H L_(A2132) H R_(C8)R_(A54) L_(A1989) R_(B6) H H L_(A2061) R_(A44) H H L_(A2133) R_(B1) HR_(A54) L_(A1990) R_(B6) R_(B1) H L_(A2062) R_(A44) R_(B1) H L_(A2134)R_(B1) R_(B1) R_(A54) L_(A1991) R_(B6) R_(B3) H L_(A2063) R_(A44) R_(B3)H L_(A2135) R_(B1) R_(B3) R_(A54) L_(A1992) R_(B6) R_(B4) H L_(A2064)R_(A44) R_(B4) H L_(A2136) R_(B1) R_(B4) R_(A54) L_(A1993) R_(B6) R_(B5)H L_(A2065) R_(A44) R_(B5) H L_(A2137) R_(B1) R_(B5) R_(A54) L_(A1994)R_(B6) R_(B6) H L_(A2066) R_(A44) R_(B6) H L_(A2138) R_(B1) R_(B6)R_(A54) L_(A1995) R_(B6) R_(B7) H L_(A2067) R_(A44) R_(B7) H L_(A2139)R_(B1) R_(B7) R_(A54) L_(A1996) R_(B6) R_(B24) H L_(A2068) R_(A44)R_(B24) H L_(A2140) R_(B1) R_(B24) R_(A54) L_(A1997) R_(B6) R_(B25) HL_(A2069) R_(A44) R_(B25) H L_(A2141) R_(B1) R_(B25) R_(A54) L_(A1998)R_(B6) R_(A3) H L_(A2070) R_(A44) R_(A3) H L_(A2142) R_(B1) R_(A3)R_(A54) L_(A1999) R_(B6) R_(A34) H L_(A2071) R_(A44) R_(A34) H L_(A2143)R_(B1) R_(A34) R_(A54) L_(A2000) R_(B6) R_(A44) H L_(A2072) R_(A44)R_(A44) H L_(A2144) R_(B1) R_(A44) R_(A54) L_(A2001) R_(B6) R_(A52) HL_(A2073) R_(A44) R_(A52) H L_(A2145) R_(B1) R_(A52) R_(A54) L_(A2002)R_(B6) R_(A53) H L_(A2074) R_(A44) R_(A53) H L_(A2146) R_(B1) R_(A53)R_(A54) L_(A2003) R_(B6) R_(A54) H L_(A2075) R_(A44) R_(A54) H L_(A2147)R_(B1) R_(A54) R_(A54) L_(A2004) R_(B6) R_(C3) H L_(A2076) R_(A44)R_(C3) H L_(A2148) R_(B1) R_(C3) R_(A54) L_(A2005) R_(B6) R_(C4) HL_(A2077) R_(A44) R_(C4) H L_(A2149) R_(B1) R_(C4) R_(A54) L_(A2006)R_(B6) R_(C8) H L_(A2078) R_(A44) R_(C8) H L_(A2150) R_(B1) R_(C8)R_(A54) L_(A2007) R_(B7) H H L_(A2079) H H R_(B1) L_(A2151) R_(A54) HR_(A54) L_(A2008) R_(B7) R_(B1) H L_(A2080) H R_(B1) R_(B1) L_(A2152)R_(A54) R_(B1) R_(A54) L_(A2009) R_(B7) R_(B3) H L_(A2081) H R_(B3)R_(B1) L_(A2153) R_(A54) R_(B3) R_(A54) L_(A2010) R_(B7) R_(B4) HL_(A2082) H R_(B4) R_(B1) L_(A2154) R_(A54) R_(B4) R_(A54) L_(A2011)R_(B7) R_(B5) H L_(A2083) H R_(B5) R_(B1) L_(A2155) R_(A54) R_(B5)R_(A54) L_(A2012) R_(B7) R_(B6) H L_(A2084) H R_(B6) R_(B1) L_(A2156)R_(A54) R_(B6) R_(A54) L_(A2013) R_(B7) R_(B7) H L_(A2085) H R_(B7)R_(B1) L_(A2157) R_(A54) R_(B7) R_(A54) L_(A2014) R_(B7) R_(B24) HL_(A2086) H R_(B24) R_(B1) L_(A2158) R_(A54) R_(B24) R_(A54) L_(A2015)R_(B7) R_(B25) H L_(A2087) H R_(B25) R_(B1) L_(A2159) R_(A54) R_(B25)R_(A54) L_(A2016) R_(B7) R_(A3) H L_(A2088) H R_(A3) R_(B1) L_(A2160)R_(A54) R_(A3) R_(A54) L_(A2017) R_(B7) R_(A34) H L_(A2089) H R_(A34)R_(B1) L_(A2161) R_(A54) R_(A34) R_(A54) L_(A2018) R_(B7) R_(A44) HL_(A2090) H R_(A44) R_(B1) L_(A2162) R_(A54) R_(A44) R_(A54) L_(A2019)R_(B7) R_(A52) H L_(A2091) H R_(A52) R_(B1) L_(A2163) R_(A54) R_(A52)R_(A54) L_(A2020) R_(B7) R_(A53) H L_(A2092) H R_(A53) R_(B1) L_(A2164)R_(A54) R_(A53) R_(A54) L_(A2021) R_(B7) R_(A54) H L_(A2093) H R_(A54)R_(B1) L_(A2165) R_(A54) R_(A54) R_(A54) L_(A2022) R_(B7) R_(C3) HL_(A2094) H R_(C3) R_(B1) L_(A2166) R_(A54) R_(C3) R_(A54) L_(A2023)R_(B7) R_(C4) H L_(A2095) H R_(C4) R_(B1) L_(A2167) R_(A54) R_(C4)R_(A54) L_(A2024) R_(B7) R_(C8) H L_(A2096) H R_(C8) R_(B1) L_(A2168)R_(A54) R_(C8) R_(A54) L_(A2025) R_(B9) H H L_(A2097) R_(B1) H R_(B1)L_(A2169) R_(B6) H R_(B1) L_(A2026) R_(B9) R_(B1) H L_(A2098) R_(B1)R_(B1) R_(B1) L_(A2170) R_(B6) R_(B1) R_(B1) L_(A2027) R_(B9) R_(B3) HL_(A2099) R_(B1) R_(B3) R_(B1) L_(A2171) R_(B6) R_(B3) R_(B1) L_(A2028)R_(B9) R_(B4) H L_(A2100) R_(B1) R_(B4) R_(B1) L_(A2172) R_(B6) R_(B4)R_(B1) L_(A2029) R_(B9) R_(B5) H L_(A2101) R_(B1) R_(B5) R_(B1)L_(A2173) R_(B6) R_(B5) R_(B1) L_(A2030) R_(B9) R_(B6) H L_(A2102)R_(B1) R_(B6) R_(B1) L_(A2174) R_(B6) R_(B6) R_(B1) L_(A2031) R_(B9)R_(B7) H L_(A2103) R_(B1) R_(B7) R_(B1) L_(A2175) R_(B6) R_(B7) R_(B1)L_(A2032) R_(B9) R_(B24) H L_(A2104) R_(B1) R_(B24) R_(B1) L_(A2176)R_(B6) R_(B24) R_(B1) L_(A2033) R_(B9) R_(B25) H L_(A2105) R_(B1)R_(B25) R_(B1) L_(A2177) R_(B6) R_(B25) R_(B1) L_(A2034) R_(B9) R_(A3) HL_(A2106) R_(B1) R_(A3) R_(B1) L_(A2178) R_(B6) R_(A3) R_(B1) L_(A2035)R_(B9) R_(A34) H L_(A2107) R_(B1) R_(A34) R_(B1) L_(A2179) R_(B6)R_(A34) R_(B1) L_(A2036) R_(B9) R_(A44) H L_(A2108) R_(B1) R_(A44)R_(B1) L_(A2180) R_(B6) R_(A44) R_(B1) L_(A2037) R_(B9) R_(A52) HL_(A2109) R_(B1) R_(A52) R_(B1) L_(A2181) R_(B6) R_(A52) R_(B1)L_(A2038) R_(B9) R_(A53) H L_(A2110) R_(B1) R_(A53) R_(B1) L_(A2182)R_(B6) R_(A53) R_(B1) L_(A2039) R_(B9) R_(A54) H L_(A2111) R_(B1)R_(A54) R_(B1) L_(A2183) R_(B6) R_(A54) R_(B1) L_(A2040) R_(B9) R_(C3) HL_(A2112) R_(B1) R_(C3) R_(B1) L_(A2184) R_(B6) R_(C3) R_(B1) L_(A2041)R_(B9) R_(C4) H L_(A2113) R_(B1) R_(C4) R_(B1) L_(A2185) R_(B6) R_(C4)R_(B1) L_(A2042) R_(B9) R_(C8) H L_(A2114) R_(B1) R_(C8) R_(B1)L_(A2186) R_(B6) R_(C8) R_(B1)

In some embodiments of Formula IA, the first ligand L_(A) is selectedfrom the group consisting of:

ligands LVII-L_(Ai) that are based on a structure of Formula LVII

ligands LVIII-L_(Ai) that are based on a structure of Formula LVIII

ligands LIX-L_(Ai) that are based on a structure of Formula LIX

ligands LX-L_(Ai) that are based on a structure of Formula LX

ligands LXI-L_(Ai) that are based on a structure of Formula LXI

wherein i is an integer from 2187 to 2402 and for each i, R¹, R¹², andR¹³ in the formulas LVII through LXI are defined as follows:

L_(Ai) R¹ R¹² R¹³ L_(Ai) R¹ R¹² R¹³ L_(Ai) R¹ R¹² R¹³ L_(A2187) R_(B3) HR_(B1) L_(A2259) R_(B6) H R_(B1) L_(A2331) R_(B6) H R_(B1) L_(A2188)R_(B3) R_(B1) R_(B1) L_(A2260) R_(B6) R_(B1) R_(B1) L_(A2332) R_(B6)R_(B1) R_(B1) L_(A2189) R_(B3) R_(B3) R_(B1) L_(A2261) R_(B6) R_(B3)R_(B1) L_(A2333) R_(B6) R_(B3) R_(B1) L_(A2190) R_(B3) R_(B4) R_(B1)L_(A2262) R_(B6) R_(B4) R_(B1) L_(A2334) R_(B6) R_(B4) R_(B1) L_(A2191)R_(B3) R_(B5) R_(B1) L_(A2263) R_(B6) R_(B5) R_(B1) L_(A2335) R_(B6)R_(B5) R_(B1) L_(A2192) R_(B3) R_(B6) R_(B1) L_(A2264) R_(B6) R_(B6)R_(B1) L_(A2336) R_(B6) R_(B6) R_(B1) L_(A2193) R_(B3) R_(B7) R_(B1)L_(A2265) R_(B6) R_(B7) R_(B1) L_(A2337) R_(B6) R_(B7) R_(B1) L_(A2194)R_(B3) R_(B24) R_(B1) L_(A2266) R_(B6) R_(B24) R_(B1) L_(A2338) R_(B6)R_(B24) R_(B1) L_(A2195) R_(B3) R_(B25) R_(B1) L_(A2267) R_(B6) R_(B25)R_(B1) L_(A2339) R_(B6) R_(B25) R_(B1) L_(A2196) R_(B3) R_(A3) R_(B1)L_(A2268) R_(B6) R_(A3) R_(B1) L_(A2340) R_(B6) R_(A3) R_(B1) L_(A2197)R_(B3) R_(A34) R_(B1) L_(A2269) R_(B6) R_(A34) R_(B1) L_(A2341) R_(B6)R_(A34) R_(B1) L_(A2198) R_(B3) R_(A44) R_(B1) L_(A2270) R_(B6) R_(A44)R_(B1) L_(A2342) R_(B6) R_(A44) R_(B1) L_(A2199) R_(B3) R_(A52) R_(B1)L_(A2271) R_(B6) R_(A52) R_(B1) L_(A2343) R_(B6) R_(A52) R_(B1)L_(A2200) R_(B3) R_(A53) R_(B1) L_(A2272) R_(B6) R_(A53) R_(B1)L_(A2344) R_(B6) R_(A53) R_(B1) L_(A2201) R_(B3) R_(A54) R_(B1)L_(A2273) R_(B6) R_(A54) R_(B1) L_(A2345) R_(B6) R_(A54) R_(B1)L_(A2202) R_(B3) R_(C3) R_(B1) L_(A2274) R_(B6) R_(C3) R_(B1) L_(A2346)R_(B6) R_(C3) R_(B1) L_(A2203) R_(B3) R_(C4) R_(B1) L_(A2275) R_(B6)R_(C4) R_(B1) L_(A2347) R_(B6) R_(C4) R_(B1) L_(A2204) R_(B3) R_(C8)R_(B1) L_(A2276) R_(B6) R_(C8) R_(B1) L_(A2348) R_(B6) R_(C8) R_(B1)L_(A2205) R_(B3) H R_(B3) L_(A2277) R_(B6) H R_(B3) L_(A2349) R_(B6) HR_(B3) L_(A2206) R_(B3) R_(B1) R_(B3) L_(A2278) R_(B6) R_(B1) R_(B3)L_(A2350) R_(B6) R_(B1) R_(B3) L_(A2207) R_(B3) R_(B3) R_(B3) L_(A2279)R_(B6) R_(B3) R_(B3) L_(A2351) R_(B6) R_(B3) R_(B3) L_(A2208) R_(B3)R_(B4) R_(B3) L_(A2280) R_(B6) R_(B4) R_(B3) L_(A2352) R_(B6) R_(B4)R_(B3) L_(A2209) R_(B3) R_(B5) R_(B3) L_(A2281) R_(B6) R_(B5) R_(B3)L_(A2353) R_(B6) R_(B5) R_(B3) L_(A2210) R_(B3) R_(B6) R_(B3) L_(A2282)R_(B6) R_(B6) R_(B3) L_(A2354) R_(B6) R_(B6) R_(B3) L_(A2211) R_(B3)R_(B7) R_(B3) L_(A2283) R_(B6) R_(B7) R_(B3) L_(A2355) R_(B6) R_(B7)R_(B3) L_(A2212) R_(B3) R_(B24) R_(B3) L_(A2284) R_(B6) R_(B24) R_(B3)L_(A2356) R_(B6) R_(B24) R_(B3) L_(A2213) R_(B3) R_(B25) R_(B3)L_(A2285) R_(B6) R_(B25) R_(B3) L_(A2357) R_(B6) R_(B25) R_(B3)L_(A2214) R_(B3) R_(A3) R_(B3) L_(A2286) R_(B6) R_(A3) R_(B3) L_(A2358)R_(B6) R_(A3) R_(B3) L_(A2215) R_(B3) R_(A34) R_(B3) L_(A2287) R_(B6)R_(A34) R_(B3) L_(A2359) R_(B6) R_(A34) R_(B3) L_(A2216) R_(B3) R_(A44)R_(B3) L_(A2288) R_(B6) R_(A44) R_(B3) L_(A2360) R_(B6) R_(A44) R_(B3)L_(A2217) R_(B3) R_(A52) R_(B3) L_(A2289) R_(B6) R_(A52) R_(B3)L_(A2361) R_(B6) R_(A52) R_(B3) L_(A2218) R_(B3) R_(A53) R_(B3)L_(A2290) R_(B6) R_(A53) R_(B3) L_(A2362) R_(B6) R_(A53) R_(B3)L_(A2219) R_(B3) R_(A54) R_(B3) L_(A2291) R_(B6) R_(A54) R_(B3)L_(A2363) R_(B6) R_(A54) R_(B3) L_(A2220) R_(B3) R_(C3) R_(B3) L_(A2292)R_(B6) R_(C3) R_(B3) L_(A2364) R_(B6) R_(C3) R_(B3) L_(A2221) R_(B3)R_(C4) R_(B3) L_(A2293) R_(B6) R_(C4) R_(B3) L_(A2365) R_(B6) R_(C4)R_(B3) L_(A2222) R_(B3) R_(C8) R_(B3) L_(A2294) R_(B6) R_(C8) R_(B3)L_(A2366) R_(B6) R_(C8) R_(B3) L_(A2223) R_(B3) H R_(C3) L_(A2295)R_(B6) H R_(C3) L_(A2367) R_(B6) H R_(C3) L_(A2224) R_(B3) R_(B1) R_(C3)L_(A2296) R_(B6) R_(B1) R_(C3) L_(A2368) R_(B6) R_(B1) R_(C3) L_(A2225)R_(B3) R_(B3) R_(C3) L_(A2297) R_(B6) R_(B3) R_(C3) L_(A2369) R_(B6)R_(B3) R_(C3) L_(A2226) R_(B3) R_(B4) R_(C3) L_(A2298) R_(B6) R_(B4)R_(C3) L_(A2370) R_(B6) R_(B4) R_(C3) L_(A2227) R_(B3) R_(B5) R_(C3)L_(A2299) R_(B6) R_(B5) R_(C3) L_(A2371) R_(B6) R_(B5) R_(C3) L_(A2228)R_(B3) R_(B6) R_(C3) L_(A2300) R_(B6) R_(B6) R_(C3) L_(A2372) R_(B6)R_(B6) R_(C3) L_(A2229) R_(B3) R_(B7) R_(C3) L_(A2301) R_(B6) R_(B7)R_(C3) L_(A2373) R_(B6) R_(B7) R_(C3) L_(A2230) R_(B3) R_(B24) R_(C3)L_(A2302) R_(B6) R_(B24) R_(C3) L_(A2374) R_(B6) R_(B24) R_(C3)L_(A2231) R_(B3) R_(B25) R_(C3) L_(A2303) R_(B6) R_(B25) R_(C3)L_(A2375) R_(B6) R_(B25) R_(C3) L_(A2232) R_(B3) R_(A3) R_(C3) L_(A2304)R_(B6) R_(A3) R_(C3) L_(A2376) R_(B6) R_(A3) R_(C3) L_(A2233) R_(B3)R_(A34) R_(C3) L_(A2305) R_(B6) R_(A34) R_(C3) L_(A2377) R_(B6) R_(A34)R_(C3) L_(A2234) R_(B3) R_(A44) R_(C3) L_(A2306) R_(B6) R_(A44) R_(C3)L_(A2378) R_(B6) R_(A44) R_(C3) L_(A2235) R_(B3) R_(A52) R_(C3)L_(A2307) R_(B6) R_(A52) R_(C3) L_(A2379) R_(B6) R_(A52) R_(C3)L_(A2236) R_(B3) R_(A53) R_(C3) L_(A2308) R_(B6) R_(A53) R_(C3)L_(A2380) R_(B6) R_(A53) R_(C3) L_(A2237) R_(B3) R_(A54) R_(C3)L_(A2309) R_(B6) R_(A54) R_(C3) L_(A2381) R_(B6) R_(A54) R_(C3)L_(A2238) R_(B3) R_(C3) R_(C3) L_(A2310) R_(B6) R_(C3) R_(C3) L_(A2382)R_(B6) R_(C3) R_(C3) L_(A2239) R_(B3) R_(C4) R_(C3) L_(A2311) R_(B6)R_(C4) R_(C3) L_(A2383) R_(B6) R_(C4) R_(C3) L_(A2240) R_(B3) R_(C8)R_(C3) L_(A2312) R_(B6) R_(C8) R_(C3) L_(A2384) R_(B6) R_(C8) R_(C3)L_(A2241) R_(B3) H R_(C4) L_(A2313) R_(B6) H R_(C4) L_(A2385) R_(B6) HR_(C4) L_(A2242) R_(B3) R_(B1) R_(C4) L_(A2314) R_(B6) R_(B1) R_(C4)L_(A2386) R_(B6) R_(B1) R_(C4) L_(A2243) R_(B3) R_(B3) R_(C4) L_(A2315)R_(B6) R_(B3) R_(C4) L_(A2387) R_(B6) R_(B3) R_(C4) L_(A2244) R_(B3)R_(B4) R_(C4) L_(A2316) R_(B6) R_(B4) R_(C4) L_(A2388) R_(B6) R_(B4)R_(C4) L_(A2245) R_(B3) R_(B5) R_(C4) L_(A2317) R_(B6) R_(B5) R_(C4)L_(A2389) R_(B6) R_(B5) R_(C4) L_(A2246) R_(B3) R_(B6) R_(C4) L_(A2318)R_(B6) R_(B6) R_(C4) L_(A2390) R_(B6) R_(B6) R_(C4) L_(A2247) R_(B3)R_(B7) R_(C4) L_(A2319) R_(B6) R_(B7) R_(C4) L_(A2391) R_(B6) R_(B7)R_(C4) L_(A2248) R_(B3) R_(B24) R_(C4) L_(A2320) R_(B6) R_(B24) R_(C4)L_(A2392) R_(B6) R_(B24) R_(C4) L_(A2249) R_(B3) R_(B25) R_(C4)L_(A2321) R_(B6) R_(B25) R_(C4) L_(A2393) R_(B6) R_(B25) R_(C4)L_(A2250) R_(B3) R_(A3) R_(C4) L_(A2322) R_(B6) R_(A3) R_(C4) L_(A2394)R_(B6) R_(A3) R_(C4) L_(A2251) R_(B3) R_(A34) R_(C4) L_(A2323) R_(B6)R_(A34) R_(C4) L_(A2395) R_(B6) R_(A34) R_(C4) L_(A2252) R_(B3) R_(A44)R_(C4) L_(A2324) R_(B6) R_(A44) R_(C4) L_(A2396) R_(B6) R_(A44) R_(C4)L_(A2253) R_(B3) R_(A52) R_(C4) L_(A2325) R_(B6) R_(A52) R_(C4)L_(A2397) R_(B6) R_(A52) R_(C4) L_(A2254) R_(B3) R_(A53) R_(C4)L_(A2326) R_(B6) R_(A53) R_(C4) L_(A2398) R_(B6) R_(A53) R_(C4)L_(A2255) R_(B3) R_(A54) R_(C4) L_(A2327) R_(B6) R_(A54) R_(C4)L_(A2399) R_(B6) R_(A54) R_(C4) L_(A2256) R_(B3) R_(C3) R_(C4) L_(A2328)R_(B6) R_(C3) R_(C4) L_(A2400) R_(B6) R_(C3) R_(C4) L_(A2257) R_(B3)R_(C4) R_(C4) L_(A2329) R_(B6) R_(C4) R_(C4) L_(A2401) R_(B6) R_(C4)R_(C4) L_(A2258) R_(B3) R_(C8) R_(C4) L_(A2330) R_(B6) R_(C8) R_(C4)L_(A2402) R_(B6) R_(C8) R_(C4)wherein R_(B1) to R_(B25) have the following structures:

wherein R_(A1) to R_(A53) have the following structures

wherein R_(C1) to R_(C11) have the following structures:

In some embodiments of Formula IA, the compound has formula Ir(L_(A))₃,Ir(L_(A))(L_(B))₂, Ir(L_(A))₂(L_(B)), Ir(L_(A))₂(L_(C)), andIr(L_(A))(L_(B))(L_(C)); and wherein each L_(A), L_(B), and L_(C) is abidentate ligand, and different from each other.

In some embodiments of the compound, L_(B) is L_(Bj) selected from thegroup consisting of: L_(B1) through L_(B1260) are based on a structureof Formula XXVII,

in which R¹, R², and R³ are defined as:

L_(Bj) R¹ R² R³ L_(Bj) R¹ R² R³ L_(Bj) R¹ R² R³ L_(B1) R^(D1) R^(D1) HL_(B421) R^(D26) R^(D21) H L_(B841) R^(D7) R^(D14) R^(D1) L_(B2) R^(D2)R^(D2) H L_(B422) R^(D26) R^(D23) H L_(B842) R^(D7) R^(D15) R^(D1)L_(B3) R^(D3) R^(D3) H L_(B423) R^(D26) R^(D24) H L_(B843) R^(D7)R^(D16) R^(D1) L_(B4) R^(D4) R^(D4) H L_(B424) R^(D26) R^(D25) HL_(B844) R^(D7) R^(D17) R^(D1) L_(B5) R^(D5) R^(D5) H L_(B425) R^(D26)R^(D27) H L_(B845) R^(D7) R^(D18) R^(D1) L_(B6) R^(D6) R^(D6) H L_(B426)R^(D26) R^(D28) H L_(B846) R^(D7) R^(D19) R^(D1) L_(B7) R^(D7) R^(D7) HL_(B427) R^(D26) R^(D29) H L_(B847) R^(D7) R^(D20) R^(D1) L_(B8) R^(D8)R^(D8) H L_(B428) R^(D26) R^(D30) H L_(B848) R^(D7) R^(D21) R^(D1)L_(B9) R^(D9) R^(D9) H L_(B429) R^(D26) R^(D31) H L_(B849) R^(D7)R^(D22) R^(D1) L_(B10) R^(D10) R^(D10) H L_(B430) R^(D26) R^(D32) HL_(B850) R^(D7) R^(D23) R^(D1) L_(B11) R^(D11) R^(D11) H L_(B431)R^(D26) R^(D33) H L_(B851) R^(D7) R^(D24) R^(D1) L_(B12) R^(D12) R^(D12)H L_(B432) R^(D26) R^(D34) H L_(B852) R^(D7) R^(D25) R^(D1) L_(B13)R^(D13) R^(D13) H L_(B433) R^(D26) R^(D35) H L_(B853) R^(D7) R^(D26)R^(D1) L_(B14) R^(D14) R^(D14) H L_(B434) R^(D26) R^(D40) H L_(B854)R^(D7) R^(D27) R^(D1) L_(B15) R^(D15) R^(D15) H L_(B435) R^(D26) R^(D41)H L_(B855) R^(D7) R^(D28) R^(D1) L_(B16) R^(D16) R^(D16) H L_(B436)R^(D26) R^(D42) H L_(B856) R^(D7) R^(D29) R^(D1) L_(B17) R^(D17) R^(D17)H L_(B437) R^(D26) R^(D64) H L_(B857) R^(D7) R^(D30) R^(D1) L_(B18)R^(D18) R^(D18) H L_(B438) R^(D26) R^(D66) H L_(B858) R^(D7) R^(D31)R^(D1) L_(B19) R^(D19) R^(D19) H L_(B439) R^(D26) R^(D68) H L_(B859)R^(D7) R^(D32) R^(D1) L_(B20) R^(D20) R^(D20) H L_(B440) R^(D26) R^(D76)H L_(B860) R^(D7) R^(D33) R^(D1) L_(B21) R^(D21) R^(D21) H L_(B441)R^(D35) R^(D5) H L_(B861) R^(D7) R^(D34) R^(D1) L_(B22) R^(D22) R^(D22)H L_(B442) R^(D35) R^(D6) H L_(B862) R^(D7) R^(D35) R^(D1) L_(B23)R^(D23) R^(D23) H L_(B443) R^(D35) R^(D9) H L_(B863) R^(D7) R^(D40)R^(D1) L_(B24) R^(D24) R^(D24) H L_(B444) R^(D35) R^(D10) H L_(B864)R^(D7) R^(D41) R^(D1) L_(B25) R^(D25) R^(D25) H L_(B445) R^(D35) R^(D12)H L_(B865) R^(D7) R^(D42) R^(D1) L_(B26) R^(D26) R^(D26) H L_(B446)R^(D35) R^(D15) H L_(B866) R^(D7) R^(D64) R^(D1) L_(B27) R^(D27) R^(D27)H L_(B447) R^(D35) R^(D16) H L_(B867) R^(D7) R^(D66) R^(D1) L_(B28)R^(D28) R^(D28) H L_(B448) R^(D35) R^(D17) H L_(B868) R^(D7) R^(D68)R^(D1) L_(B29) R^(D29) R^(D29) H L_(B449) R^(D35) R^(D18) H L_(B869)R^(D7) R^(D76) R^(D1) L_(B30) R^(D30) R^(D30) H L_(B450) R^(D35) R^(D19)H L_(B870) R^(D8) R^(D5) R^(D1) L_(B31) R^(D31) R^(D31) H L_(B451)R^(D35) R^(D20) H L_(B871) R^(D8) R^(D6) R^(D1) L_(B32) R^(D32) R^(D32)H L_(B452) R^(D35) R^(D21) H L_(B872) R^(D8) R^(D9) R^(D1) L_(B33)R^(D33) R^(D33) H L_(B453) R^(D35) R^(D22) H L_(B873) R^(D8) R^(D10)R^(D1) L_(B34) R^(D34) R^(D34) H L_(B454) R^(D35) R^(D23) H L_(B874)R^(D8) R^(D11) R^(D1) L_(B35) R^(D35) R^(D35) H L_(B455) R^(D35) R^(D24)H L_(B875) R^(D8) R^(D12) R^(D1) L_(B36) R^(D40) R^(D40) H L_(B456)R^(D35) R^(D27) H L_(B876) R^(D8) R^(D13) R^(D1) L_(B37) R^(D41) R^(D41)H L_(B457) R^(D35) R^(D28) H L_(B877) R^(D8) R^(D14) R^(D1) L_(B38)R^(D42) R^(D42) H L_(B458) R^(D35) R^(D29) H L_(B878) R^(D8) R^(D15)R^(D1) L_(B39) R^(D64) R^(D64) H L_(B459) R^(D35) R^(D30) H L_(B879)R^(D8) R^(D16) R^(D1) L_(B40) R^(D66) R^(D66) H L_(B460) R^(D35) R^(D31)H L_(B880) R^(D8) R^(D17) R^(D1) L_(B41) R^(D68) R^(D68) H L_(B461)R^(D35) R^(D32) H L_(B881) R^(D8) R^(D18) R^(D1) L_(B42) R^(D76) R^(D76)H L_(B462) R^(D35) R^(D33) H L_(B882) R^(D8) R^(D19) R^(D1) L_(B43)R^(D1) R^(D2) H L_(B463) R^(D35) R^(D34) H L_(B883) R^(D8) R^(D20)R^(D1) L_(B44) R^(D1) R^(D3) H L_(B464) R^(D35) R^(D40) H L_(B884)R^(D8) R^(D21) R^(D1) L_(B45) R^(D1) R^(D4) H L_(B465) R^(D35) R^(D41) HL_(B885) R^(D8) R^(D22) R^(D1) L_(B46) R^(D1) R^(D5) H L_(B466) R^(D35)R^(D42) H L_(B886) R^(D8) R^(D23) R^(D1) L_(B47) R^(D1) R^(D6) HL_(B467) R^(D35) R^(D64) H L_(B887) R^(D8) R^(D24) R^(D1) L_(B48) R^(D1)R^(D7) H L_(B468) R^(D35) R^(D66) H L_(B888) R^(D8) R^(D25) R^(D1)L_(B49) R^(D1) R^(D8) H L_(B469) R^(D35) R^(D68) H L_(B889) R^(D8)R^(D26) R^(D1) L_(B50) R^(D1) R^(D9) H L_(B470) R^(D35) R^(D76) HL_(B890) R^(D8) R^(D27) R^(D1) L_(B51) R^(D1) R^(D10) H L_(B471) R^(D40)R^(D5) H L_(B891) R^(D8) R^(D28) R^(D1) L_(B52) R^(D1) R^(D11) HL_(B472) R^(D40) R^(D6) H L_(B892) R^(D8) R^(D29) R^(D1) L_(B53) R^(D1)R^(D12) H L_(B473) R^(D40) R^(D9) H L_(B893) R^(D8) R^(D30) R^(D1)L_(B54) R^(D1) R^(D13) H L_(B474) R^(D40) R^(D10) H L_(B894) R^(D8)R^(D31) R^(D1) L_(B55) R^(D1) R^(D14) H L_(B475) R^(D40) R^(D12) HL_(B895) R^(D8) R^(D32) R^(D1) L_(B56) R^(D1) R^(D15) H L_(B476) R^(D40)R^(D15) H L_(B896) R^(D8) R^(D33) R^(D1) L_(B57) R^(D1) R^(D16) HL_(B477) R^(D40) R^(D16) H L_(B897) R^(D8) R^(D34) R^(D1) L_(B58) R^(D1)R^(D17) H L_(B478) R^(D40) R^(D17) H L_(B898) R^(D8) R^(D35) R^(D1)L_(B59) R^(D1) R^(D18) H L_(B479) R^(D40) R^(D18) H L_(B899) R^(D8)R^(D40) R^(D1) L_(B60) R^(D1) R^(D19) H L_(B480) R^(D40) R^(D19) HL_(B900) R^(D8) R^(D41) R^(D1) L_(B61) R^(D1) R^(D20) H L_(B481) R^(D40)R^(D20) H L_(B901) R^(D8) R^(D42) R^(D1) L_(B62) R^(D1) R^(D21) HL_(B482) R^(D40) R^(D21) H L_(B902) R^(D8) R^(D64) R^(D1) L_(B63) R^(D1)R^(D22) H L_(B483) R^(D40) R^(D23) H L_(B903) R^(D8) R^(D66) R^(D1)L_(B64) R^(D1) R^(D23) H L_(B484) R^(D40) R^(D24) H L_(B904) R^(D8)R^(D68) R^(D1) L_(B65) R^(D1) R^(D24) H L_(B485) R^(D40) R^(D25) HL_(B905) R^(D8) R^(D76) R^(D1) L_(B66) R^(D1) R^(D25) H L_(B486) R^(D40)R^(D27) H L_(B906) R^(D11) R^(D5) R^(D1) L_(B67) R^(D1) R^(D26) HL_(B487) R^(D40) R^(D28) H L_(B907) R^(D11) R^(D6) R^(D1) L_(B68) R^(D1)R^(D27) H L_(B488) R^(D40) R^(D29) H L_(B908) R^(D11) R^(D9) R^(D1)L_(B69) R^(D1) R^(D28) H L_(B489) R^(D40) R^(D30) H L_(B909) R^(D11)R^(D10) R^(D1) L_(B70) R^(D1) R^(D29) H L_(B490) R^(D40) R^(D31) HL_(B910) R^(D11) R^(D12) R^(D1) L_(B71) R^(D1) R^(D30) H L_(B491)R^(D40) R^(D32) H L_(B911) R^(D11) R^(D13) R^(D1) L_(B72) R^(D1) R^(D31)H L_(B492) R^(D40) R^(D33) H L_(B912) R^(D11) R^(D14) R^(D1) L_(B73)R^(D1) R^(D32) H L_(B493) R^(D40) R^(D34) H L_(B913) R^(D11) R^(D15)R^(D1) L_(B74) R^(D1) R^(D33) H L_(B494) R^(D40) R^(D41) H L_(B914)R^(D11) R^(D16) R^(D1) L_(B75) R^(D1) R^(D34) H L_(B495) R^(D40) R^(D42)H L_(B915) R^(D11) R^(D17) R^(D1) L_(B76) R^(D1) R^(D35) H L_(B496)R^(D40) R^(D64) H L_(B916) R^(D11) R^(D18) R^(D1) L_(B77) R^(D1) R^(D40)H L_(B497) R^(D40) R^(D66) H L_(B917) R^(D11) R^(D19) R^(D1) L_(B78)R^(D1) R^(D41) H L_(B498) R^(D40) R^(D68) H L_(B918) R^(D11) R^(D20)R^(D1) L_(B79) R^(D1) R^(D42) H L_(B499) R^(D40) R^(D76) H L_(B919)R^(D11) R^(D21) R^(D1) L_(B80) R^(D1) R^(D64) H L_(B500) R^(D41) R^(D5)H L_(B920) R^(D11) R^(D22) R^(D1) L_(B81) R^(D1) R^(D66) H L_(B501)R^(D41) R^(D6) H L_(B921) R^(D11) R^(D23) R^(D1) L_(B82) R^(D1) R^(D68)H L_(B502) R^(D41) R^(D9) H L_(B922) R^(D11) R^(D24) R^(D1) L_(B83)R^(D1) R^(D76) H L_(B503) R^(D41) R^(D10) H L_(B923) R^(D11) R^(D25)R^(D1) L_(B84) R^(D2) R^(D1) H L_(B504) R^(D41) R^(D12) H L_(B924)R^(D11) R^(D26) R^(D1) L_(B85) R^(D2) R^(D3) H L_(B505) R^(D41) R^(D15)H L_(B925) R^(D11) R^(D27) R^(D1) L_(B86) R^(D2) R^(D4) H L_(B506)R^(D41) R^(D16) H L_(B926) R^(D11) R^(D28) R^(D1) L_(B87) R^(D2) R^(D5)H L_(B507) R^(D41) R^(D17) H L_(B927) R^(D11) R^(D29) R^(D1) L_(B88)R^(D2) R^(D6) H L_(B508) R^(D41) R^(D18) H L_(B928) R^(D11) R^(D30)R^(D1) L_(B89) R^(D2) R^(D7) H L_(B509) R^(D41) R^(D19) H L_(B929)R^(D11) R^(D31) R^(D1) L_(B90) R^(D2) R^(D8) H L_(B510) R^(D41) R^(D20)H L_(B930) R^(D11) R^(D32) R^(D1) L_(B91) R^(D2) R^(D9) H L_(B511)R^(D41) R^(D21) H L_(B931) R^(D11) R^(D33) R^(D1) L_(B92) R^(D2) R^(D10)H L_(B512) R^(D41) R^(D22) H L_(B932) R^(D11) R^(D34) R^(D1) L_(B93)R^(D2) R^(D11) H L_(B513) R^(D41) R^(D23) H L_(B933) R^(D11) R^(D35)R^(D1) L_(B94) R^(D2) R^(D12) H L_(B514) R^(D41) R^(D24) H L_(B934)R^(D11) R^(D40) R^(D1) L_(B95) R^(D2) R^(D13) H L_(B515) R^(D41) R^(D25)H L_(B935) R^(D11) R^(D41) R^(D1) L_(B96) R^(D2) R^(D14) H L_(B516)R^(D41) R^(D26) H L_(B936) R^(D11) R^(D42) R^(D1) L_(B97) R^(D2) R^(D15)H L_(B517) R^(D41) R^(D27) H L_(B937) R^(D11) R^(D64) R^(D1) L_(B98)R^(D2) R^(D16) H L_(B518) R^(D41) R^(D28) H L_(B938) R^(D11) R^(D66)R^(D1) L_(B99) R^(D2) R^(D17) H L_(B519) R^(D41) R^(D29) H L_(B939)R^(D11) R^(D68) R^(D1) L_(B100) R^(D2) R^(D18) H L_(B520) R^(D41)R^(D30) H L_(B940) R^(D11) R^(D76) R^(D1) L_(B101) R^(D2) R^(D19) HL_(B521) R^(D41) R^(D31) H L_(B941) R^(D13) R^(D5) R^(D1) L_(B102)R^(D2) R^(D20) H L_(B522) R^(D41) R^(D32) H L_(B942) R^(D13) R^(D6)R^(D1) L_(B103) R^(D2) R^(D21) H L_(B523) R^(D41) R^(D42) H L_(B943)R^(D13) R^(D9) R^(D1) L_(B104) R^(D2) R^(D22) H L_(B524) R^(D41) R^(D64)H L_(B944) R^(D13) R^(D10) R^(D1) L_(B105) R^(D2) R^(D23) H L_(B525)R^(D41) R^(D66) H L_(B945) R^(D13) R^(D12) R^(D1) L_(B106) R^(D2)R^(D24) H L_(B526) R^(D41) R^(D68) H L_(B946) R^(D13) R^(D14) R^(D1)L_(B107) R^(D2) R^(D25) H L_(B527) R^(D41) R^(D76) H L_(B947) R^(D13)R^(D15) R^(D1) L_(B108) R^(D2) R^(D26) H L_(B528) R^(D64) R^(D5) HL_(B948) R^(D13) R^(D16) R^(D1) L_(B109) R^(D2) R^(D27) H L_(B529)R^(D64) R^(D6) H L_(B949) R^(D13) R^(D17) R^(D1) L_(B110) R^(D2) R^(D28)H L_(B530) R^(D64) R^(D9) H L_(B950) R^(D13) R^(D18) R^(D1) L_(B111)R^(D2) R^(D29) H L_(B531) R^(D64) R^(D10) H L_(B951) R^(D13) R^(D19)R^(D1) L_(B112) R^(D2) R^(D30) H L_(B532) R^(D64) R^(D12) H L_(B952)R^(D13) R^(D20) R^(D1) L_(B113) R^(D2) R^(D31) H L_(B533) R^(D64)R^(D15) H L_(B953) R^(D13) R^(D21) R^(D1) L_(B114) R^(D2) R^(D32) HL_(B534) R^(D64) R^(D16) H L_(B954) R^(D13) R^(D22) R^(D1) L_(B115)R^(D2) R^(D33) H L_(B535) R^(D64) R^(D17) H L_(B955) R^(D13) R^(D23)R^(D1) L_(B116) R^(D2) R^(D34) H L_(B536) R^(D64) R^(D18) H L_(B956)R^(D13) R^(D24) R^(D1) L_(B117) R^(D2) R^(D35) H L_(B537) R^(D64)R^(D19) H L_(B957) R^(D13) R^(D25) R^(D1) L_(B118) R^(D2) R^(D40) HL_(B538) R^(D64) R^(D20) H L_(B958) R^(D13) R^(D26) R^(D1) L_(B119)R^(D2) R^(D41) H L_(B539) R^(D64) R^(D21) H L_(B959) R^(D13) R^(D27)R^(D1) L_(B120) R^(D2) R^(D42) H L_(B540) R^(D64) R^(D23) H L_(B960)R^(D13) R^(D28) R^(D1) L_(B121) R^(D2) R^(D64) H L_(B541) R^(D64)R^(D24) H L_(B961) R^(D13) R^(D29) R^(D1) L_(B122) R^(D2) R^(D66) HL_(B542) R^(D64) R^(D25) H L_(B962) R^(D13) R^(D30) R^(D1) L_(B123)R^(D2) R^(D68) H L_(B543) R^(D64) R^(D27) H L_(B963) R^(D13) R^(D31)R^(D1) L_(B124) R^(D2) R^(D76) H L_(B544) R^(D64) R^(D28) H L_(B964)R^(D13) R^(D32) R^(D1) L_(B125) R^(D3) R^(D4) H L_(B545) R^(D64) R^(D29)H L_(B965) R^(D13) R^(D33) R^(D1) L_(B126) R^(D3) R^(D5) H L_(B546)R^(D64) R^(D30) H L_(B966) R^(D13) R^(D34) R^(D1) L_(B127) R^(D3) R^(D6)H L_(B547) R^(D64) R^(D31) H L_(B967) R^(D13) R^(D35) R^(D1) L_(B128)R^(D3) R^(D7) H L_(B548) R^(D64) R^(D32) H L_(B968) R^(D13) R^(D40)R^(D1) L_(B129) R^(D3) R^(D8) H L_(B549) R^(D64) R^(D33) H L_(B969)R^(D13) R^(D41) R^(D1) L_(B130) R^(D3) R^(D9) H L_(B550) R^(D64) R^(D34)H L_(B970) R^(D13) R^(D42) R^(D1) L_(B131) R^(D3) R^(D10) H L_(B551)R^(D64) R^(D42) H L_(B971) R^(D13) R^(D64) R^(D1) L_(B132) R^(D3)R^(D11) H L_(B552) R^(D64) R^(D64) H L_(B972) R^(D13) R^(D66) R^(D1)L_(B133) R^(D3) R^(D12) H L_(B553) R^(D64) R^(D66) H L_(B973) R^(D13)R^(D68) R^(D1) L_(B134) R^(D3) R^(D13) H L_(B554) R^(D64) R^(D68) HL_(B974) R^(D13) R^(D76) R^(D1) L_(B135) R^(D3) R^(D14) H L_(B555)R^(D64) R^(D76) H L_(B975) R^(D14) R^(D5) R^(D1) L_(B136) R^(D3) R^(D15)H L_(B556) R^(D66) R^(D5) H L_(B976) R^(D14) R^(D6) R^(D1) L_(B137)R^(D3) R^(D16) H L_(B557) R^(D66) R^(D6) H L_(B977) R^(D14) R^(D9)R^(D1) L_(B138) R^(D3) R^(D17) H L_(B558) R^(D66) R^(D9) H L_(B978)R^(D14) R^(D10) R^(D1) L_(B139) R^(D3) R^(D18) H L_(B559) R^(D66)R^(D10) H L_(B979) R^(D14) R^(D12) R^(D1) L_(B140) R^(D3) R^(D19) HL_(B560) R^(D66) R^(D12) H L_(B980) R^(D14) R^(D15) R^(D1) L_(B141)R^(D3) R^(D20) H L_(B561) R^(D66) R^(D15) H L_(B981) R^(D14) R^(D16)R^(D1) L_(B142) R^(D3) R^(D21) H L_(B562) R^(D66) R^(D16) H L_(B982)R^(D14) R^(D17) R^(D1) L_(B143) R^(D3) R^(D22) H L_(B563) R^(D66)R^(D17) H L_(B983) R^(D14) R^(D18) R^(D1) L_(B144) R^(D3) R^(D23) HL_(B564) R^(D66) R^(D18) H L_(B984) R^(D14) R^(D19) R^(D1) L_(B145)R^(D3) R^(D24) H L_(B565) R^(D66) R^(D19) H L_(B985) R^(D14) R^(D20)R^(D1) L_(B146) R^(D3) R^(D25) H L_(B566) R^(D66) R^(D20) H L_(B986)R^(D14) R^(D21) R^(D1) L_(B147) R^(D3) R^(D26) H L_(B567) R^(D66)R^(D21) H L_(B987) R^(D14) R^(D22) R^(D1) L_(B148) R^(D3) R^(D27) HL_(B568) R^(D66) R^(D23) H L_(B988) R^(D14) R^(D23) R^(D1) L_(B149)R^(D3) R^(D28) H L_(B569) R^(D66) R^(D24) H L_(B989) R^(D14) R^(D24)R^(D1) L_(B150) R^(D3) R^(D29) H L_(B570) R^(D66) R^(D25) H L_(B990)R^(D14) R^(D25) R^(D1) L_(B151) R^(D3) R^(D30) H L_(B571) R^(D66)R^(D27) H L_(B991) R^(D14) R^(D26) R^(D1) L_(B152) R^(D3) R^(D31) HL_(B572) R^(D66) R^(D28) H L_(B992) R^(D14) R^(D27) R^(D1) L_(B153)R^(D3) R^(D32) H L_(B573) R^(D66) R^(D29) H L_(B993) R^(D14) R^(D28)R^(D1) L_(B154) R^(D3) R^(D33) H L_(B574) R^(D66) R^(D30) H L_(B994)R^(D14) R^(D29) R^(D1) L_(B155) R^(D3) R^(D34) H L_(B575) R^(D66)R^(D31) H L_(B995) R^(D14) R^(D30) R^(D1) L_(B156) R^(D3) R^(D35) HL_(B576) R^(D66) R^(D32) H L_(B996) R^(D14) R^(D31) R^(D1) L_(B157)R^(D3) R^(D40) H L_(B577) R^(D66) R^(D33) H L_(B997) R^(D14) R^(D32)R^(D1) L_(B158) R^(D3) R^(D41) H L_(B578) R^(D66) R^(D34) H L_(B998)R^(D14) R^(D33) R^(D1) L_(B159) R^(D3) R^(D42) H L_(B579) R^(D66)R^(D42) H L_(B999) R^(D14) R^(D34) R^(D1) L_(B160) R^(D3) R^(D64) HL_(B580) R^(D66) R^(D68) H L_(B1000) R^(D14) R^(D35) R^(D1) L_(B161)R^(D3) R^(D66) H L_(B581) R^(D66) R^(D76) H L_(B1001) R^(D14) R^(D40)R^(D1) L_(B162) R^(D3) R^(D68) H L_(B582) R^(D68) R^(D5) H L_(B1002)R^(D14) R^(D41) R^(D1) L_(B163) R^(D3) R^(D76) H L_(B583) R^(D68) R^(D6)H L_(B1003) R^(D14) R^(D42) R^(D1) L_(B164) R^(D4) R^(D5) H L_(B584)R^(D68) R^(D9) H L_(B1004) R^(D14) R^(D64) R^(D1) L_(B165) R^(D4) R^(D6)H L_(B585) R^(D68) R^(D10) H L_(B1005) R^(D14) R^(D66) R^(D1) L_(B166)R^(D4) R^(D7) H L_(B586) R^(D68) R^(D12) H L_(B1006) R^(D14) R^(D68)R^(D1) L_(B167) R^(D4) R^(D8) H L_(B587) R^(D68) R^(D15) H L_(B1007)R^(D14) R^(D76) R^(D1) L_(B168) R^(D4) R^(D9) H L_(B588) R^(D68) R^(D16)H L_(B1008) R^(D22) R^(D5) R^(D1) L_(B169) R^(D4) R^(D10) H L_(B589)R^(D68) R^(D17) H L_(B1009) R^(D22) R^(D6) R^(D1) L_(B170) R^(D4)R^(D11) H L_(B590) R^(D68) R^(D18) H L_(B1010) R^(D22) R^(D9) R^(D1)L_(B171) R^(D4) R^(D12) H L_(B591) R^(D68) R^(D19) H L_(B1011) R^(D22)R^(D10) R^(D1) L_(B172) R^(D4) R^(D13) H L_(B592) R^(D68) R^(D20) HL_(B1012) R^(D22) R^(D12) R^(D1) L_(B173) R^(D4) R^(D14) H L_(B593)R^(D68) R^(D21) H L_(B1013) R^(D22) R^(D15) R^(D1) L_(B174) R^(D4)R^(D15) H L_(B594) R^(D68) R^(D23) H L_(B1014) R^(D22) R^(D16) R^(D1)L_(B175) R^(D4) R^(D16) H L_(B595) R^(D68) R^(D24) H L_(B1015) R^(D22)R^(D17) R^(D1) L_(B176) R^(D4) R^(D17) H L_(B596) R^(D68) R^(D25) HL_(B1016) R^(D22) R^(D18) R^(D1) L_(B177) R^(D4) R^(D18) H L_(B597)R^(D68) R^(D27) H L_(B1017) R^(D22) R^(D19) R^(D1) L_(B178) R^(D4)R^(D19) H L_(B598) R^(D68) R^(D28) H L_(B1018) R^(D22) R^(D20) R^(D1)L_(B179) R^(D4) R^(D20) H L_(B599) R^(D68) R^(D29) H L_(B1019) R^(D22)R^(D21) R^(D1) L_(B180) R^(D4) R^(D21) H L_(B600) R^(D68) R^(D30) HL_(B1020) R^(D22) R^(D23) R^(D1) L_(B181) R^(D4) R^(D22) H L_(B601)R^(D68) R^(D31) H L_(B1021) R^(D22) R^(D24) R^(D1) L_(B182) R^(D4)R^(D23) H L_(B602) R^(D68) R^(D32) H L_(B1022) R^(D22) R^(D25) R^(D1)L_(B183) R^(D4) R^(D24) H L_(B603) R^(D68) R^(D33) H L_(B1023) R^(D22)R^(D26) R^(D1) L_(B184) R^(D4) R^(D25) H L_(B604) R^(D68) R^(D34) HL_(B1024) R^(D22) R^(D27) R^(D1) L_(B185) R^(D4) R^(D26) H L_(B605)R^(D68) R^(D42) H L_(B1025) R^(D22) R^(D28) R^(D1) L_(B186) R^(D4)R^(D27) H L_(B606) R^(D68) R^(D76) H L_(B1026) R^(D22) R^(D29) R^(D1)L_(B187) R^(D4) R^(D28) H L_(B607) R^(D76) R^(D5) H L_(B1027) R^(D22)R^(D30) R^(D1) L_(B188) R^(D4) R^(D29) H L_(B608) R^(D76) R^(D6) HL_(B1028) R^(D22) R^(D31) R^(D1) L_(B189) R^(D4) R^(D30) H L_(B609)R^(D76) R^(D9) H L_(B1029) R^(D22) R^(D32) R^(D1) L_(B190) R^(D4)R^(D31) H L_(B610) R^(D76) R^(D10) H L_(B1030) R^(D22) R^(D33) R^(D1)L_(B191) R^(D4) R^(D32) H L_(B611) R^(D76) R^(D12) H L_(B1031) R^(D22)R^(D34) R^(D1) L_(B192) R^(D4) R^(D33) H L_(B612) R^(D76) R^(D15) HL_(B1032) R^(D22) R^(D35) R^(D1) L_(B193) R^(D4) R^(D34) H L_(B613)R^(D76) R^(D16) H L_(B1033) R^(D22) R^(D40) R^(D1) L_(B194) R^(D4)R^(D35) H L_(B614) R^(D76) R^(D17) H L_(B1034) R^(D22) R^(D41) R^(D1)L_(B195) R^(D4) R^(D40) H L_(B615) R^(D76) R^(D18) H L_(B1035) R^(D22)R^(D42) R^(D1) L_(B196) R^(D4) R^(D41) H L_(B616) R^(D76) R^(D19) HL_(B1036) R^(D22) R^(D64) R^(D1) L_(B197) R^(D4) R^(D42) H L_(B617)R^(D76) R^(D20) H L_(B1037) R^(D22) R^(D66) R^(D1) L_(B198) R^(D4)R^(D64) H L_(B618) R^(D76) R^(D21) H L_(B1038) R^(D22) R^(D68) R^(D1)L_(B199) R^(D4) R^(D66) H L_(B619) R^(D76) R^(D23) H L_(B1039) R^(D22)R^(D76) R^(D1) L_(B200) R^(D4) R^(D68) H L_(B620) R^(D76) R^(D24) HL_(B1040) R^(D26) R^(D5) R^(D1) L_(B201) R^(D4) R^(D76) H L_(B621)R^(D76) R^(D25) H L_(B1041) R^(D26) R^(D6) R^(D1) L_(B202) R^(D4) R^(D1)H L_(B622) R^(D76) R^(D27) H L_(B1042) R^(D26) R^(D9) R^(D1) L_(B203)R^(D7) R^(D5) H L_(B623) R^(D76) R^(D28) H L_(B1043) R^(D26) R^(D10)R^(D1) L_(B204) R^(D7) R^(D6) H L_(B624) R^(D76) R^(D29) H L_(B1044)R^(D26) R^(D12) R^(D1) L_(B205) R^(D7) R^(D8) H L_(B625) R^(D76) R^(D30)H L_(B1045) R^(D26) R^(D15) R^(D1) L_(B206) R^(D7) R^(D9) H L_(B626)R^(D76) R^(D31) H L_(B1046) R^(D26) R^(D16) R^(D1) L_(B207) R^(D7)R^(D10) H L_(B627) R^(D76) R^(D32) H L_(B1047) R^(D26) R^(D17) R^(D1)L_(B208) R^(D7) R^(D11) H L_(B628) R^(D76) R^(D33) H L_(B1048) R^(D26)R^(D18) R^(D1) L_(B209) R^(D7) R^(D12) H L_(B629) R^(D76) R^(D34) HL_(B1049) R^(D26) R^(D19) R^(D1) L_(B210) R^(D7) R^(D13) H L_(B630)R^(D76) R^(D42) H L_(B1050) R^(D26) R^(D20) R^(D1) L_(B211) R^(D7)R^(D14) H L_(B631) R^(D1) R^(D1) R^(D1) L_(B1051) R^(D26) R^(D21) R^(D1)L_(B212) R^(D7) R^(D15) H L_(B632) R^(D2) R^(D2) R^(D1) L_(B1052)R^(D26) R^(D23) R^(D1) L_(B213) R^(D7) R^(D16) H L_(B633) R^(D3) R^(D3)R^(D1) L_(B1053) R^(D26) R^(D24) R^(D1) L_(B214) R^(D7) R^(D17) HL_(B634) R^(D4) R^(D4) R^(D1) L_(B1054) R^(D26) R^(D25) R^(D1) L_(B215)R^(D7) R^(D18) H L_(B635) R^(D5) R^(D5) R^(D1) L_(B1055) R^(D26) R^(D27)R^(D1) L_(B216) R^(D7) R^(D19) H L_(B636) R^(D6) R^(D6) R^(D1) L_(B1056)R^(D26) R^(D28) R^(D1) L_(B217) R^(D7) R^(D20) H L_(B637) R^(D7) R^(D7)R^(D1) L_(B1057) R^(D26) R^(D29) R^(D1) L_(B218) R^(D7) R^(D21) HL_(B638) R^(D8) R^(D8) R^(D1) L_(B1058) R^(D26) R^(D30) R^(D1) L_(B219)R^(D7) R^(D22) H L_(B639) R^(D9) R^(D9) R^(D1) L_(B1059) R^(D26) R^(D31)R^(D1) L_(B220) R^(D7) R^(D23) H L_(B640) R^(D10) R^(D10) R^(D1)L_(B1060) R^(D26) R^(D32) R^(D1) L_(B221) R^(D7) R^(D24) H L_(B641)R^(D11) R^(D11) R^(D1) L_(B1061) R^(D26) R^(D33) R^(D1) L_(B222) R^(D7)R^(D25) H L_(B642) R^(D12) R^(D12) R^(D1) L_(B1062) R^(D26) R^(D34)R^(D1) L_(B223) R^(D7) R^(D26) H L_(B643) R^(D13) R^(D13) R^(D1)L_(B1063) R^(D26) R^(D35) R^(D1) L_(B224) R^(D7) R^(D27) H L_(B644)R^(D14) R^(D14) R^(D1) L_(B1064) R^(D26) R^(D40) R^(D1) L_(B225) R^(D7)R^(D28) H L_(B645) R^(D15) R^(D15) R^(D1) L_(B1065) R^(D26) R^(D41)R^(D1) L_(B226) R^(D7) R^(D29) H L_(B646) R^(D16) R^(D16) R^(D1)L_(B1066) R^(D26) R^(D42) R^(D1) L_(B227) R^(D7) R^(D30) H L_(B647)R^(D17) R^(D17) R^(D1) L_(B1067) R^(D26) R^(D64) R^(D1) L_(B228) R^(D7)R^(D31) H L_(B648) R^(D18) R^(D18) R^(D1) L_(B1068) R^(D26) R^(D66)R^(D1) L_(B229) R^(D7) R^(D32) H L_(B649) R^(D19) R^(D19) R^(D1)L_(B1069) R^(D26) R^(D68) R^(D1) L_(B230) R^(D7) R^(D33) H L_(B650)R^(D20) R^(D20) R^(D1) L_(B1070) R^(D26) R^(D76) R^(D1) L_(B231) R^(D7)R^(D34) H L_(B651) R^(D21) R^(D21) R^(D1) L_(B1071) R^(D35) R^(D5)R^(D1) L_(B232) R^(D7) R^(D35) H L_(B652) R^(D22) R^(D22) R^(D1)L_(B1072) R^(D35) R^(D6) R^(D1) L_(B233) R^(D7) R^(D40) H L_(B653)R^(D23) R^(D23) R^(D1) L_(B1073) R^(D35) R^(D9) R^(D1) L_(B234) R^(D7)R^(D41) H L_(B654) R^(D24) R^(D24) R^(D1) L_(B1074) R^(D35) R^(D10)R^(D1) L_(B235) R^(D7) R^(D42) H L_(B655) R^(D25) R^(D25) R^(D1)L_(B1075) R^(D35) R^(D12) R^(D1) L_(B236) R^(D7) R^(D64) H L_(B656)R^(D26) R^(D26) R^(D1) L_(B1076) R^(D35) R^(D15) R^(D1) L_(B237) R^(D7)R^(D66) H L_(B657) R^(D27) R^(D27) R^(D1) L_(B1077) R^(D35) R^(D16)R^(D1) L_(B238) R^(D7) R^(D68) H L_(B658) R^(D28) R^(D28) R^(D1)L_(B1078) R^(D35) R^(D17) R^(D1) L_(B239) R^(D7) R^(D76) H L_(B659)R^(D29) R^(D29) R^(D1) L_(B1079) R^(D35) R^(D18) R^(D1) L_(B240) R^(D8)R^(D5) H L_(B660) R^(D30) R^(D30) R^(D1) L_(B1080) R^(D35) R^(D19)R^(D1) L_(B241) R^(D8) R^(D6) H L_(B661) R^(D31) R^(D31) R^(D1)L_(B1081) R^(D35) R^(D20) R^(D1) L_(B242) R^(D8) R^(D9) H L_(B662)R^(D32) R^(D32) R^(D1) L_(B1082) R^(D35) R^(D21) R^(D1) L_(B243) R^(D8)R^(D10) H L_(B663) R^(D33) R^(D33) R^(D1) L_(B1083) R^(D35) R^(D23)R^(D1) L_(B244) R^(D8) R^(D11) H L_(B664) R^(D34) R^(D34) R^(D1)L_(B1084) R^(D35) R^(D24) R^(D1) L_(B245) R^(D8) R^(D12) H L_(B665)R^(D35) R^(D35) R^(D1) L_(B1085) R^(D35) R^(D25) R^(D1) L_(B246) R^(D8)R^(D13) H L_(B666) R^(D40) R^(D40) R^(D1) L_(B1086) R^(D35) R^(D27)R^(D1) L_(B247) R^(D8) R^(D14) H L_(B667) R^(D41) R^(D41) R^(D1)L_(B1087) R^(D35) R^(D28) R^(D1) L_(B248) R^(D8) R^(D15) H L_(B668)R^(D42) R^(D42) R^(D1) L_(B1088) R^(D35) R^(D29) R^(D1) L_(B249) R^(D8)R^(D16) H L_(B669) R^(D64) R^(D64) R^(D1) L_(B1089) R^(D35) R^(D30)R^(D1) L_(B250) R^(D8) R^(D17) H L_(B670) R^(D66) R^(D66) R^(D1)L_(B1090) R^(D35) R^(D31) R^(D1) L_(B251) R^(D8) R^(D18) H L_(B671)R^(D68) R^(D68) R^(D1) L_(B1091) R^(D35) R^(D32) R^(D1) L_(B252) R^(D8)R^(D19) H L_(B672) R^(D76) R^(D76) R^(D1) L_(B1092) R^(D35) R^(D33)R^(D1) L_(B253) R^(D8) R^(D20) H L_(B673) R^(D1) R^(D2) R^(D1) L_(B1093)R^(D35) R^(D34) R^(D1) L_(B254) R^(D8) R^(D21) H L_(B674) R^(D1) R^(D3)R^(D1) L_(B1094) R^(D35) R^(D40) R^(D1) L_(B255) R^(D8) R^(D22) HL_(B675) R^(D1) R^(D4) R^(D1) L_(B1095) R^(D35) R^(D41) R^(D1) L_(B256)R^(D8) R^(D23) H L_(B676) R^(D1) R^(D5) R^(D1) L_(B1096) R^(D35) R^(D42)R^(D1) L_(B257) R^(D8) R^(D24) H L_(B677) R^(D1) R^(D6) R^(D1) L_(B1097)R^(D35) R^(D64) R^(D1) L_(B258) R^(D8) R^(D25) H L_(B678) R^(D1) R^(D7)R^(D1) L_(B1098) R^(D35) R^(D66) R^(D1) L_(B259) R^(D8) R^(D26) HL_(B679) R^(D1) R^(D8) R^(D1) L_(B1099) R^(D35) R^(D68) R^(D1) L_(B260)R^(D8) R^(D27) H L_(B680) R^(D1) R^(D9) R^(D1) L_(B1100) R^(D35) R^(D76)R^(D1) L_(B261) R^(D8) R^(D28) H L_(B681) R^(D1) R^(D10) R^(D1)L_(B1101) R^(D40) R^(D5) R^(D1) L_(B262) R^(D8) R^(D29) H L_(B682)R^(D1) R^(D11) R^(D1) L_(B1102) R^(D40) R^(D6) R^(D1) L_(B263) R^(D8)R^(D30) H L_(B683) R^(D1) R^(D12) R^(D1) L_(B1103) R^(D40) R^(D9) R^(D1)L_(B264) R^(D8) R^(D31) H L_(B684) R^(D1) R^(D13) R^(D1) L_(B1104)R^(D40) R^(D10) R^(D1) L_(B265) R^(D8) R^(D32) H L_(B685) R^(D1) R^(D14)R^(D1) L_(B1105) R^(D40) R^(D12) R^(D1) L_(B266) R^(D8) R^(D33) HL_(B686) R^(D1) R^(D15) R^(D1) L_(B1106) R^(D40) R^(D15) R^(D1) L_(B267)R^(D8) R^(D34) H L_(B687) R^(D1) R^(D16) R^(D1) L_(B1107) R^(D40)R^(D16) R^(D1) L_(B268) R^(D8) R^(D35) H L_(B688) R^(D1) R^(D17) R^(D1)L_(B1108) R^(D40) R^(D17) R^(D1) L_(B269) R^(D8) R^(D40) H L_(B689)R^(D1) R^(D18) R^(D1) L_(B1109) R^(D40) R^(D18) R^(D1) L_(B270) R^(D8)R^(D41) H L_(B690) R^(D1) R^(D19) R^(D1) L_(B1110) R^(D40) R^(D19)R^(D1) L_(B271) R^(D8) R^(D42) H L_(B691) R^(D1) R^(D20) R^(D1)L_(B1111) R^(D40) R^(D20) R^(D1) L_(B272) R^(D8) R^(D64) H L_(B692)R^(D1) R^(D21) R^(D1) L_(B1112) R^(D40) R^(D21) R^(D1) L_(B273) R^(D8)R^(D66) H L_(B693) R^(D1) R^(D22) R^(D1) L_(B1113) R^(D40) R^(D23)R^(D1) L_(B274) R^(D8) R^(D68) H L_(B694) R^(D1) R^(D23) R^(D1)L_(B1114) R^(D40) R^(D24) R^(D1) L_(B275) R^(D8) R^(D76) H L_(B695)R^(D1) R^(D24) R^(D1) L_(B1115) R^(D40) R^(D25) R^(D1) L_(B276) R^(D11)R^(D5) H L_(B696) R^(D1) R^(D25) R^(D1) L_(B1116) R^(D40) R^(D27) R^(D1)L_(B277) R^(D11) R^(D6) H L_(B697) R^(D1) R^(D26) R^(D1) L_(B1117)R^(D40) R^(D28) R^(D1) L_(B278) R^(D11) R^(D9) H L_(B698) R^(D1) R^(D27)R^(D1) L_(B1118) R^(D40) R^(D29) R^(D1) L_(B279) R^(D11) R^(D10) HL_(B699) R^(D1) R^(D28) R^(D1) L_(B1119) R^(D40) R^(D30) R^(D1) L_(B280)R^(D11) R^(D12) H L_(B700) R^(D1) R^(D29) R^(D1) L_(B1120) R^(D40)R^(D31) R^(D1) L_(B281) R^(D11) R^(D13) H L_(B701) R^(D1) R^(D30) R^(D1)L_(B1121) R^(D40) R^(D32) R^(D1) L_(B282) R^(D11) R^(D14) H L_(B702)R^(D1) R^(D31) R^(D1) L_(B1122) R^(D40) R^(D33) R^(D1) L_(B283) R^(D11)R^(D15) H L_(B703) R^(D1) R^(D32) R^(D1) L_(B1123) R^(D40) R^(D34)R^(D1) L_(B284) R^(D11) R^(D16) H L_(B704) R^(D1) R^(D33) R^(D1)L_(B1124) R^(D40) R^(D41) R^(D1) L_(B285) R^(D11) R^(D17) H L_(B705)R^(D1) R^(D34) R^(D1) L_(B1125) R^(D40) R^(D42) R^(D1) L_(B286) R^(D11)R^(D18) H L_(B706) R^(D1) R^(D35) R^(D1) L_(B1126) R^(D40) R^(D64)R^(D1) L_(B287) R^(D11) R^(D19) H L_(B707) R^(D1) R^(D40) R^(D1)L_(B1127) R^(D40) R^(D66) R^(D1) L_(B288) R^(D11) R^(D20) H L_(B708)R^(D1) R^(D41) R^(D1) L_(B1128) R^(D40) R^(D68) R^(D1) L_(B289) R^(D11)R^(D21) H L_(B709) R^(D1) R^(D42) R^(D1) L_(B1129) R^(D40) R^(D76)R^(D1) L_(B290) R^(D11) R^(D22) H L_(B710) R^(D1) R^(D64) R^(D1)L_(B1130) R^(D41) R^(D5) R^(D1) L_(B291) R^(D11) R^(D23) H L_(B711)R^(D1) R^(D66) R^(D1) L_(B1131) R^(D41) R^(D6) R^(D1) L_(B292) R^(D11)R^(D24) H L_(B712) R^(D1) R^(D68) R^(D1) L_(B1132) R^(D41) R^(D9) R^(D1)L_(B293) R^(D11) R^(D25) H L_(B713) R^(D1) R^(D76) R^(D1) L_(B1133)R^(D41) R^(D10) R^(D1) L_(B294) R^(D11) R^(D26) H L_(B714) R^(D2) R^(D1)R^(D1) L_(B1134) R^(D41) R^(D12) R^(D1) L_(B295) R^(D11) R^(D27) HL_(B715) R^(D2) R^(D3) R^(D1) L_(B1135) R^(D41) R^(D15) R^(D1) L_(B296)R^(D11) R^(D28) H L_(B716) R^(D2) R^(D4) R^(D1) L_(B1136) R^(D41)R^(D16) R^(D1) L_(B297) R^(D11) R^(D29) H L_(B717) R^(D2) R^(D5) R^(D1)L_(B1137) R^(D41) R^(D17) R^(D1) L_(B298) R^(D11) R^(D30) H L_(B718)R^(D2) R^(D6) R^(D1) L_(B1138) R^(D41) R^(D18) R^(D1) L_(B299) R^(D11)R^(D31) H L_(B719) R^(D2) R^(D7) R^(D1) L_(B1139) R^(D41) R^(D19) R^(D1)L_(B300) R^(D11) R^(D32) H L_(B720) R^(D2) R^(D8) R^(D1) L_(B1140)R^(D41) R^(D20) R^(D1) L_(B301) R^(D11) R^(D33) H L_(B721) R^(D2) R^(D9)R^(D1) L_(B1141) R^(D41) R^(D21) R^(D1) L_(B302) R^(D11) R^(D34) HL_(B722) R^(D2) R^(D10) R^(D1) L_(B1142) R^(D41) R^(D23) R^(D1) L_(B303)R^(D11) R^(D35) H L_(B723) R^(D2) R^(D11) R^(D1) L_(B1143) R^(D41)R^(D24) R^(D1) L_(B304) R^(D11) R^(D40) H L_(B724) R^(D2) R^(D12) R^(D1)L_(B1144) R^(D41) R^(D25) R^(D1) L_(B305) R^(D11) R^(D41) H L_(B725)R^(D2) R^(D13) R^(D1) L_(B1145) R^(D41) R^(D27) R^(D1) L_(B306) R^(D11)R^(D42) H L_(B726) R^(D2) R^(D14) R^(D1) L_(B1146) R^(D41) R^(D28)R^(D1) L_(B307) R^(D11) R^(D64) H L_(B727) R^(D2) R^(D15) R^(D1)L_(B1147) R^(D41) R^(D29) R^(D1) L_(B308) R^(D11) R^(D66) H L_(B728)R^(D2) R^(D16) R^(D1) L_(B1148) R^(D41) R^(D30) R^(D1) L_(B309) R^(D11)R^(D68) H L_(B729) R^(D2) R^(D17) R^(D1) L_(B1149) R^(D41) R^(D31)R^(D1) L_(B310) R^(D11) R^(D76) H L_(B730) R^(D2) R^(D18) R^(D1)L_(B1150) R^(D41) R^(D32) R^(D1) L_(B311) R^(D13) R^(D5) H L_(B731)R^(D2) R^(D19) R^(D1) L_(B1151) R^(D41) R^(D33) R^(D1) L_(B312) R^(D13)R^(D6) H L_(B732) R^(D2) R^(D20) R^(D1) L_(B1152) R^(D41) R^(D34) R^(D1)L_(B313) R^(D13) R^(D9) H L_(B733) R^(D2) R^(D21) R^(D1) L_(B1153)R^(D41) R^(D42) R^(D1) L_(B314) R^(D13) R^(D10) H L_(B734) R^(D2)R^(D22) R^(D1) L_(B1154) R^(D41) R^(D64) R^(D1) L_(B315) R^(D13) R^(D12)H L_(B735) R^(D2) R^(D23) R^(D1) L_(B1155) R^(D41) R^(D66) R^(D1)L_(B316) R^(D13) R^(D14) H L_(B736) R^(D2) R^(D24) R^(D1) L_(B1156)R^(D41) R^(D68) R^(D1) L_(B317) R^(D13) R^(D15) H L_(B737) R^(D2)R^(D25) R^(D1) L_(B1157) R^(D41) R^(D76) R^(D1) L_(B318) R^(D13) R^(D16)H L_(B738) R^(D2) R^(D26) R^(D1) L_(B1158) R^(D64) R^(D5) R^(D1)L_(B319) R^(D13) R^(D17) H L_(B739) R^(D2) R^(D27) R^(D1) L_(B1159)R^(D64) R^(D6) R^(D1) L_(B320) R^(D13) R^(D18) H L_(B740) R^(D2) R^(D28)R^(D1) L_(B1160) R^(D64) R^(D9) R^(D1) L_(B321) R^(D13) R^(D19) HL_(B741) R^(D2) R^(D29) R^(D1) L_(B1161) R^(D64) R^(D10) R^(D1) L_(B322)R^(D13) R^(D20) H L_(B742) R^(D2) R^(D30) R^(D1) L_(B1162) R^(D64)R^(D12) R^(D1) L_(B323) R^(D13) R^(D21) H L_(B743) R^(D2) R^(D31) R^(D1)L_(B1163) R^(D64) R^(D15) R^(D1) L_(B324) R^(D13) R^(D22) H L_(B744)R^(D2) R^(D32) R^(D1) L_(B1164) R^(D64) R^(D16) R^(D1) L_(B325) R^(D13)R^(D23) H L_(B745) R^(D2) R^(D33) R^(D1) L_(B1165) R^(D64) R^(D17)R^(D1) L_(B326) R^(D13) R^(D24) H L_(B746) R^(D2) R^(D34) R^(D1)L_(B1166) R^(D64) R^(D18) R^(D1) L_(B327) R^(D13) R^(D25) H L_(B747)R^(D2) R^(D35) R^(D1) L_(B1167) R^(D64) R^(D19) R^(D1) L_(B328) R^(D13)R^(D26) H L_(B748) R^(D2) R^(D40) R^(D1) L_(B1168) R^(D64) R^(D20)R^(D1) L_(B329) R^(D13) R^(D27) H L_(B749) R^(D2) R^(D41) R^(D1)L_(B1169) R^(D64) R^(D21) R^(D1) L_(B330) R^(D13) R^(D28) H L_(B750)R^(D2) R^(D42) R^(D1) L_(B1170) R^(D64) R^(D23) R^(D1) L_(B331) R^(D13)R^(D29) H L_(B751) R^(D2) R^(D64) R^(D1) L_(B1171) R^(D64) R^(D24)R^(D1) L_(B332) R^(D13) R^(D30) H L_(B752) R^(D2) R^(D66) R^(D1)L_(B1172) R^(D64) R^(D25) R^(D1) L_(B333) R^(D13) R^(D31) H L_(B753)R^(D2) R^(D68) R^(D1) L_(B1173) R^(D64) R^(D27) R^(D1) L_(B334) R^(D13)R^(D32) H L_(B754) R^(D2) R^(D76) R^(D1) L_(B1174) R^(D64) R^(D28)R^(D1) L_(B335) R^(D13) R^(D33) H L_(B755) R^(D3) R^(D4) R^(D1)L_(B1175) R^(D64) R^(D29) R^(D1) L_(B336) R^(D13) R^(D34) H L_(B756)R^(D3) R^(D5) R^(D1) L_(B1176) R^(D64) R^(D30) R^(D1) L_(B337) R^(D13)R^(D35) H L_(B757) R^(D3) R^(D6) R^(D1) L_(B1177) R^(D64) R^(D31) R^(D1)L_(B338) R^(D13) R^(D40) H L_(B758) R^(D3) R^(D7) R^(D1) L_(B1178)R^(D64) R^(D32) R^(D1) L_(B339) R^(D13) R^(D41) H L_(B759) R^(D3) R^(D8)R^(D1) L_(B1179) R^(D64) R^(D33) R^(D1) L_(B340) R^(D13) R^(D42) HL_(B760) R^(D3) R^(D9) R^(D1) L_(B1180) R^(D64) R^(D34) R^(D1) L_(B341)R^(D13) R^(D64) H L_(B761) R^(D3) R^(D10) R^(D1) L_(B1181) R^(D64)R^(D42) R^(D1) L_(B342) R^(D13) R^(D66) H L_(B762) R^(D3) R^(D11) R^(D1)L_(B1182) R^(D64) R^(D64) R^(D1) L_(B343) R^(D13) R^(D68) H L_(B763)R^(D3) R^(D12) R^(D1) L_(B1183) R^(D64) R^(D66) R^(D1) L_(B344) R^(D13)R^(D76) H L_(B764) R^(D3) R^(D13) R^(D1) L_(B1184) R^(D64) R^(D68)R^(D1) L_(B345) R^(D14) R^(D5) H L_(B765) R^(D3) R^(D14) R^(D1)L_(B1185) R^(D64) R^(D76) R^(D1) L_(B346) R^(D14) R^(D6) H L_(B766)R^(D3) R^(D15) R^(D1) L_(B1186) R^(D66) R^(D5) R^(D1) L_(B347) R^(D14)R^(D9) H L_(B767) R^(D3) R^(D16) R^(D1) L_(B1187) R^(D66) R^(D6) R^(D1)L_(B348) R^(D14) R^(D10) H L_(B768) R^(D3) R^(D17) R^(D1) L_(B1188)R^(D66) R^(D9) R^(D1) L_(B349) R^(D14) R^(D12) H L_(B769) R^(D3) R^(D18)R^(D1) L_(B1189) R^(D66) R^(D10) R^(D1) L_(B350) R^(D14) R^(D15) HL_(B770) R^(D3) R^(D19) R^(D1) L_(B1190) R^(D66) R^(D12) R^(D1) L_(B351)R^(D14) R^(D16) H L_(B771) R^(D3) R^(D20) R^(D1) L_(B1191) R^(D66)R^(D15) R^(D1) L_(B352) R^(D14) R^(D17) H L_(B772) R^(D3) R^(D21) R^(D1)L_(B1192) R^(D66) R^(D16) R^(D1) L_(B353) R^(D14) R^(D18) H L_(B773)R^(D3) R^(D22) R^(D1) L_(B1193) R^(D66) R^(D17) R^(D1) L_(B354) R^(D14)R^(D19) H L_(B774) R^(D3) R^(D23) R^(D1) L_(B1194) R^(D66) R^(D18)R^(D1) L_(B355) R^(D14) R^(D20) H L_(B775) R^(D3) R^(D24) R^(D1)L_(B1195) R^(D66) R^(D19) R^(D1) L_(B356) R^(D14) R^(D21) H L_(B776)R^(D3) R^(D25) R^(D1) L_(B1196) R^(D66) R^(D20) R^(D1) L_(B357) R^(D14)R^(D22) H L_(B777) R^(D3) R^(D26) R^(D1) L_(B1197) R^(D66) R^(D21)R^(D1) L_(B358) R^(D14) R^(D23) H L_(B778) R^(D3) R^(D27) R^(D1)L_(B1198) R^(D66) R^(D23) R^(D1) L_(B359) R^(D14) R^(D24) H L_(B779)R^(D3) R^(D28) R^(D1) L_(B1199) R^(D66) R^(D24) R^(D1) L_(B360) R^(D14)R^(D25) H L_(B780) R^(D3) R^(D29) R^(D1) L_(B1200) R^(D66) R^(D25)R^(D1) L_(B361) R^(D14) R^(D26) H L_(B781) R^(D3) R^(D30) R^(D1)L_(B1201) R^(D66) R^(D27) R^(D1) L_(B362) R^(D14) R^(D27) H L_(B782)R^(D3) R^(D31) R^(D1) L_(B1202) R^(D66) R^(D28) R^(D1) L_(B363) R^(D14)R^(D28) H L_(B783) R^(D3) R^(D32) R^(D1) L_(B1203) R^(D66) R^(D29)R^(D1) L_(B364) R^(D14) R^(D29) H L_(B784) R^(D3) R^(D33) R^(D1)L_(B1204) R^(D66) R^(D30) R^(D1) L_(B365) R^(D14) R^(D30) H L_(B785)R^(D3) R^(D34) R^(D1) L_(B1205) R^(D66) R^(D31) R^(D1) L_(B366) R^(D14)R^(D31) H L_(B786) R^(D3) R^(D35) R^(D1) L_(B1206) R^(D66) R^(D32)R^(D1) L_(B367) R^(D14) R^(D32) H L_(B787) R^(D3) R^(D40) R^(D1)L_(B1207) R^(D66) R^(D33) R^(D1) L_(B368) R^(D14) R^(D33) H L_(B788)R^(D3) R^(D41) R^(D1) L_(B1208) R^(D66) R^(D34) R^(D1) L_(B369) R^(D14)R^(D34) H L_(B789) R^(D3) R^(D42) R^(D1) L_(B1209) R^(D66) R^(D42)R^(D1) L_(B370) R^(D14) R^(D35) H L_(B790) R^(D3) R^(D64) R^(D1)L_(B1210) R^(D66) R^(D68) R^(D1) L_(B371) R^(D14) R^(D40) H L_(B791)R^(D3) R^(D66) R^(D1) L_(B1211) R^(D66) R^(D76) R^(D1) L_(B372) R^(D14)R^(D41) H L_(B792) R^(D3) R^(D68) R^(D1) L_(B1212) R^(D68) R^(D5) R^(D1)L_(B373) R^(D14) R^(D42) H L_(B793) R^(D3) R^(D76) R^(D1) L_(B1213)R^(D68) R^(D6) R^(D1) L_(B374) R^(D14) R^(D64) H L_(B794) R^(D4) R^(D5)R^(D1) L_(B1214) R^(D68) R^(D9) R^(D1) L_(B375) R^(D14) R^(D66) HL_(B795) R^(D4) R^(D6) R^(D1) L_(B1215) R^(D68) R^(D10) R^(D1) L_(B376)R^(D14) R^(D68) H L_(B796) R^(D4) R^(D7) R^(D1) L_(B1216) R^(D68)R^(D12) R^(D1) L_(B377) R^(D14) R^(D76) H L_(B797) R^(D4) R^(D8) R^(D1)L_(B1217) R^(D68) R^(D15) R^(D1) L_(B378) R^(D22) R^(D5) H L_(B798)R^(D4) R^(D9) R^(D1) L_(B1218) R^(D68) R^(D16) R^(D1) L_(B379) R^(D22)R^(D6) H L_(B799) R^(D4) R^(D10) R^(D1) L_(B1219) R^(D68) R^(D17) R^(D1)L_(B380) R^(D22) R^(D9) H L_(B800) R^(D4) R^(D11) R^(D1) L_(B1220)R^(D68) R^(D18) R^(D1) L_(B381) R^(D22) R^(D10) H L_(B801) R^(D4)R^(D12) R^(D1) L_(B1221) R^(D68) R^(D19) R^(D1) L_(B382) R^(D22) R^(D12)H L_(B802) R^(D4) R^(D13) R^(D1) L_(B1222) R^(D68) R^(D20) R^(D1)L_(B383) R^(D22) R^(D15) H L_(B803) R^(D4) R^(D14) R^(D1) L_(B1223)R^(D68) R^(D21) R^(D1) L_(B384) R^(D22) R^(D16) H L_(B804) R^(D4)R^(D15) R^(D1) L_(B1224) R^(D68) R^(D23) R^(D1) L_(B385) R^(D22) R^(D17)H L_(B805) R^(D4) R^(D16) R^(D1) L_(B1225) R^(D68) R^(D24) R^(D1)L_(B386) R^(D22) R^(D18) H L_(B806) R^(D4) R^(D17) R^(D1) L_(B1226)R^(D68) R^(D25) R^(D1) L_(B387) R^(D22) R^(D19) H L_(B807) R^(D4)R^(D18) R^(D1) L_(B1227) R^(D68) R^(D27) R^(D1) L_(B388) R^(D22) R^(D20)H L_(B808) R^(D4) R^(D19) R^(D1) L_(B1228) R^(D68) R^(D28) R^(D1)L_(B389) R^(D22) R^(D21) H L_(B809) R^(D4) R^(D20) R^(D1) L_(B1229)R^(D68) R^(D29) R^(D1) L_(B390) R^(D22) R^(D23) H L_(B810) R^(D4)R^(D21) R^(D1) L_(B1230) R^(D68) R^(D30) R^(D1) L_(B391) R^(D22) R^(D24)H L_(B811) R^(D4) R^(D22) R^(D1) L_(B1231) R^(D68) R^(D31) R^(D1)L_(B392) R^(D22) R^(D25) H L_(B812) R^(D4) R^(D23) R^(D1) L_(B1232)R^(D68) R^(D32) R^(D1) L_(B393) R^(D22) R^(D26) H L_(B813) R^(D4)R^(D24) R^(D1) L_(B1233) R^(D68) R^(D33) R^(D1) L_(B394) R^(D22) R^(D27)H L_(B814) R^(D4) R^(D25) R^(D1) L_(B1234) R^(D68) R^(D34) R^(D1)L_(B395) R^(D22) R^(D28) H L_(B815) R^(D4) R^(D26) R^(D1) L_(B1235)R^(D68) R^(D42) R^(D1) L_(B396) R^(D22) R^(D29) H L_(B816) R^(D4)R^(D27) R^(D1) L_(B1236) R^(D68) R^(D76) R^(D1) L_(B397) R^(D22) R^(D30)H L_(B817) R^(D4) R^(D28) R^(D1) L_(B1237) R^(D76) R^(D5) R^(D1)L_(B398) R^(D22) R^(D31) H L_(B818) R^(D4) R^(D29) R^(D1) L_(B1238)R^(D76) R^(D6) R^(D1) L_(B399) R^(D22) R^(D32) H L_(B819) R^(D4) R^(D30)R^(D1) L_(B1239) R^(D76) R^(D9) R^(D1) L_(B400) R^(D22) R^(D33) HL_(B820) R^(D4) R^(D31) R^(D1) L_(B1240) R^(D76) R^(D10) R^(D1) L_(B401)R^(D22) R^(D34) H L_(B821) R^(D4) R^(D32) R^(D1) L_(B1241) R^(D76)R^(D12) R^(D1) L_(B402) R^(D22) R^(D35) H L_(B822) R^(D4) R^(D33) R^(D1)L_(B1242) R^(D76) R^(D15) R^(D1) L_(B403) R^(D22) R^(D40) H L_(B823)R^(D4) R^(D34) R^(D1) L_(B1243) R^(D76) R^(D16) R^(D1) L_(B404) R^(D22)R^(D41) H L_(B824) R^(D4) R^(D35) R^(D1) L_(B1244) R^(D76) R^(D17)R^(D1) L_(B405) R^(D22) R^(D42) H L_(B825) R^(D4) R^(D40) R^(D1)L_(B1245) R^(D76) R^(D18) R^(D1) L_(B406) R^(D22) R^(D64) H L_(B826)R^(D4) R^(D41) R^(D1) L_(B1246) R^(D76) R^(D19) R^(D1) L_(B407) R^(D22)R^(D66) H L_(B827) R^(D4) R^(D42) R^(D1) L_(B1247) R^(D76) R^(D20)R^(D1) L_(B408) R^(D22) R^(D68) H L_(B828) R^(D4) R^(D64) R^(D1)L_(B1248) R^(D76) R^(D21) R^(D1) L_(B409) R^(D22) R^(D76) H L_(B829)R^(D4) R^(D66) R^(D1) L_(B1249) R^(D76) R^(D23) R^(D1) L_(B410) R^(D26)R^(D5) H L_(B830) R^(D4) R^(D68) R^(D1) L_(B1250) R^(D76) R^(D24) R^(D1)L_(B411) R^(D26) R^(D6) H L_(B831) R^(D4) R^(D76) R^(D1) L_(B1251)R^(D76) R^(D25) R^(D1) L_(B412) R^(D26) R^(D9) H L_(B832) R^(D4) R^(D1)R^(D1) L_(B1252) R^(D76) R^(D27) R^(D1) L_(B413) R^(D26) R^(D10) HL_(B833) R^(D7) R^(D5) R^(D1) L_(B1253) R^(D76) R^(D28) R^(D1) L_(B414)R^(D26) R^(D12) H L_(B834) R^(D7) R^(D6) R^(D1) L_(B1254) R^(D76)R^(D29) R^(D1) L_(B415) R^(D26) R^(D15) H L_(B835) R^(D7) R^(D8) R^(D1)L_(B1255) R^(D76) R^(D30) R^(D1) L_(B416) R^(D26) R^(D16) H L_(B836)R^(D7) R^(D9) R^(D1) L_(B1256) R^(D76) R^(D31) R^(D1) L_(B417) R^(D26)R^(D17) H L_(B837) R^(D7) R^(D10) R^(D1) L_(B1257) R^(D76) R^(D32)R^(D1) L_(B418) R^(D26) R^(D18) H L_(B838) R^(D7) R^(D11) R^(D1)L_(B1258) R^(D76) R^(D33) R^(D1) L_(B419) R^(D26) R^(D19) H L_(B839)R^(D7) R^(D12) R^(D1) L_(B1259) R^(D76) R^(D34) R^(D1) L_(B420) R^(D26)R^(D20) H L_(B840) R^(D7) R^(D13) R^(D1) L_(B1260) R^(D76) R^(D42)R^(D1)wherein R^(D1) to R^(D81) has the following structures:

In some embodiments, the compound is Compound Z-x having the formulaIr(Z-L_(Ai))₂(L_(Bj)), wherein Z is Roman numerals from I to LXI;

where x=1260i+j−1260, j is an integer from 1 to 1260; where for Z is 1to XII, i is an integer from 1 to 618; where for Z is XIII to XVII, i isan integer from 619 to 1170; where for Z is XVIII to XLIV, and LXII toLXV, i is an integer from 1171 to 1584; where for Z is XLV to LI, i isan integer from 1585 to 1970; where for Z is LII to LVI, i is an integerfrom 1971 to 2186; where for Z is LVII to LXI, i is an integer from 2187to 2402; where each corresponding L_(Ai) and L_(Bj) are defined above.

The OLEDs and the Devices of the Present Disclosure

In another aspect, the present disclosure also provides an OLEDcomprising a first organic layer that contains a compound as disclosedin the above compounds section of the present disclosure. In someembodiments, the OLED comprises: an anode; a cathode; and an organiclayer disposed between the anode and the cathode, wherein the organiclayer comprises a compound comprising a ligand L_(A) of Formula I,Formula IA defined above, Formula II, Formula III, or Formula IV:

wherein: ring B is independently a 5-membered or 6-membered carbocyclicor heterocyclic ring; X¹ to X⁴ are each independently selected from thegroup consisting of C, N, and CR; at least one pair of adjacent X¹ to X⁴are each C and fused to a structure of Formula V

where indicated by “

”; X⁵ to X¹² are each independently C or N; the maximum number of Nwithin a ring is two; Z and Y are each independently selected from thegroup consisting of O, S, Se, NR′, CR′R″, SiR′R″, and GeR′R″; R^(B) andR^(C) each independently represents zero, mono, or up to a maximumallowed substitutions to its associated ring; each of R^(B), R^(C), R,R′, and R″ is independently a hydrogen or a substituent selected fromthe group consisting of the general substituents defined herein; and twosubstituents can be joined or fused to form a ring; the ligand L_(A) iscomplexed to a metal M through the two indicated dash lines of eachFormula; and the ligand L_(A) can be joined with other ligands to form atridentate, tetradentate, pentadentate, or hexadentate ligand.

In some embodiments, the OLED has one or more characteristics selectedfrom the group consisting of being flexible, being rollable, beingfoldable, being stretchable, and being curved. In some embodiments, theOLED is transparent or semi-transparent. In some embodiments, the OLEDfurther comprises a layer comprising carbon nanotubes.

In some embodiments, the OLED further comprises a layer comprising adelayed fluorescent emitter. In some embodiments, the OLED comprises aRGB pixel arrangement or white plus color filter pixel arrangement. Insome embodiments, the OLED is a mobile device, a hand held device, or awearable device. In some embodiments, the OLED is a display panel havingless than 10 inch diagonal or 50 square inch area. In some embodiments,the OLED is a display panel having at least 10 inch diagonal or 50square inch area. In some embodiments, the OLED is a lighting panel.

In some embodiments, the compound can be an emissive dopant. In someembodiments, the compound can produce emissions via phosphorescence,fluorescence, thermally activated delayed fluorescence, i.e., TADF (alsoreferred to as E-type delayed fluorescence; see, e.g., U.S. applicationSer. No. 15/700,352, published on Mar. 14, 2019 as U.S. patentapplication publication No. 2019/0081248, which is hereby incorporatedby reference in its entirety), triplet-triplet annihilation, orcombinations of these processes. In some embodiments, the emissivedopant can be a racemic mixture, or can be enriched in one enantiomer.In some embodiments, the compound can be homoleptic (each ligand is thesame). In some embodiments, the compound can be heteroleptic (at leastone ligand is different from others).

When there are more than one ligand coordinated to a metal, the ligandscan all be the same in some embodiments. In some other embodiments, atleast one ligand is different from the other ligand(s). In someembodiments, every ligand can be different from each other. This is alsotrue in embodiments where a ligand being coordinated to a metal can belinked with other ligands being coordinated to that metal to form atridentate, tetradentate, pentadentate, or hexadentate ligands Thus,where the coordinating ligands are being linked together, all of theligands can be the same in some embodiments, and at least one of theligands being linked can be different from the other ligand(s) in someother embodiments.

In some embodiments, the compound can be used as a phosphorescentsensitizer in an OLED where one or multiple layers in the OLED containsan acceptor in the form of one or more fluorescent and/or delayedfluorescence emitters. In some embodiments, the compound can be used asone component of an exciplex to be used as a sensitizer. As aphosphorescent sensitizer, the compound must be capable of energytransfer to the acceptor and the acceptor will emit the energy orfurther transfer energy to a final emitter. The acceptor concentrationscan range from 0.001% to 100%. The acceptor could be in either the samelayer as the phosphorescent sensitizer or in one or more differentlayers. In some embodiments, the acceptor is a TADF emitter. In someembodiments, the acceptor is a fluorescent emitter. In some embodiments,the emission can arise from any or all of the sensitizer, acceptor, andfinal emitter

In some embodiments, the compound of the present disclosure is neutrallycharged.

According to another aspect, a formulation comprising the compounddescribed herein is also disclosed.

The OLED disclosed herein can be incorporated into one or more of aconsumer product, an electronic component module, and a lighting panel.The organic layer can be an emissive layer and the compound can be anemissive dopant in some embodiments, while the compound can be anon-emissive dopant in other embodiments.

The organic layer can also include a host. In some embodiments, two ormore hosts are preferred. In some embodiments, the hosts used maybe a)bipolar, b) electron transporting, c) hole transporting or d) wide bandgap materials that play little role in charge transport. In someembodiments, the host can include a metal complex. The host can be atriphenylene containing benzo-fused thiophene or benzo-fused furan. Anysubstituent in the host can be an unfused substituent independentlyselected from the group consisting of C_(n)H_(2n+1), OC_(n)H_(2n+1),OAr₁, N(C_(n)H_(2n+1))₂, N(Ar₁)(Ar₂), CH═CH—C_(n)H_(2n+1),C≡C—C_(n)H_(2n+1), Ar₁, Ar₁—Ar₂, and C_(n)H_(2n)—Ar₁, or the host has nosubstitutions. In the preceding substituents n can range from 1 to 10;and Ar₁ and Ar₂ can be independently selected from the group consistingof benzene, biphenyl, naphthalene, triphenylene, carbazole, andheteroaromatic analogs thereof. The host can be an inorganic compound,for example, a Zn containing inorganic material e.g. ZnS.

The host can be a compound comprising at least one chemical groupselected from the group consisting of triphenylene, carbazole,dibenzothiophene, dibenzofuran, dibenzoselenophene, azatriphenylene,azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, andaza-dibenzoselenophene. The host can include a metal complex. The hostcan be, but is not limited to, a specific compound selected from theHost Group consisting of:

and combinations thereof.Additional information on possible hosts is provided below.

In some embodiments, the emissive region may comprise a compoundcomprising a ligand L_(A) of Formula I, Formula IA defined above,Formula II, Formula III, or Formula IV:

wherein:ring B is independently a 5-membered or 6-membered carbocyclic orheterocyclic ring; X¹ to X⁴ are each independently selected from thegroup consisting of C, N, and CR; at least one pair of adjacent X¹ to X⁴are each C and fused to a structure of Formula V

where indicated by “

”; X⁵ to X¹² are each independently C or N; the maximum number of Nwithin a ring is two; Z and Y are each independently selected from thegroup consisting of O, S, Se, NR′, CR′R″, SiR′R″, and GeR′R″; R^(B) andR^(C) each independently represents zero, mono, or up to a maximumallowed substitutions to its associated ring; each of R^(B), R^(C), R,R′, and R″ is independently hydrogen or a substituent selected from thegroup consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl,heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl,cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylicacid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl,phosphino, boryl, and combinations thereof; and two substituents can bejoined or fused to form a ring; the ligand L_(A) is complexed to a metalM through the two indicated dash lines of each Formula; and the ligandL_(A) can be joined with other ligands to form a tridentate,tetradentate, pentadentate, or hexadentate ligand.

In some embodiments of the emissive region, the compound can be anemissive dopant or a non-emissive dopant.

In some embodiments of the emissive region, the emissive region furthercomprises a host, wherein host contains at least one chemical groupselected from the group consisting of metal complex, triphenylene,carbazole, dibenzothiophene, dibenzofuran, dibenzoselenophene,aza-triphenylene, aza-carbazole, aza-dibenzothiophene, aza-dibenzofuran,and aza-dibenzoselenophene.

In some embodiments, the host may be selected from the group consistingof the HOST Group defined herein.

According to another aspect, a consumer product comprising an OLED isdisclosed, wherein the OLED comprises: an anode; a cathode; and anorganic layer disposed between the anode and the cathode, wherein theorganic layer comprises a compound comprising a ligand L_(A) of FormulaI, Formula IA defined above, Formula II, Formula III, or Formula IV:

wherein:ring B is independently a 5-membered or 6-membered carbocyclic orheterocyclic ring; X¹ to X⁴ are each independently selected from thegroup consisting of C, N, and CR; at least one pair of adjacent X¹ to X⁴are each C and fused to a structure of Formula V

where indicated by “

”; X⁵ to X¹² are each independently C or N; the maximum number of Nwithin a ring is two; Z and Y are each independently selected from thegroup consisting of O, S, Se, NR′, CR′R″, SiR′R″, and GeR′R″; R^(B) andR^(C) each independently represents zero, mono, or up to a maximumallowed substitutions to its associated ring; each of R^(B), R^(C), R,R′, and R″ is independently hydrogen or a substituent selected from thegroup consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl,heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl,cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylicacid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl,phosphino, boryl, and combinations thereof; and two substituents can bejoined or fused to form a ring; the ligand L_(A) is complexed to a metalM through the two indicated dash lines of each Formula; and the ligandL_(A) can be joined with other ligands to form a tridentate,tetradentate, pentadentate, or hexadentate ligand.

In yet another aspect of the present disclosure, a formulation thatcomprises the novel compound disclosed herein is described. Theformulation can include one or more components selected from the groupconsisting of a solvent, a host, a hole injection material, holetransport material, electron blocking material, hole blocking material,and an electron transport material, disclosed herein.

The present disclosure encompasses any chemical structure comprising thenovel compound of the present disclosure, or a monovalent or polyvalentvariant thereof. In other words, the inventive compound, or a monovalentor polyvalent variant thereof, can be a part of a larger chemicalstructure. Such chemical structure can be selected from the groupconsisting of a monomer, a polymer, a macromolecule, and a supramolecule(also known as supermolecule). As used herein, a “monovalent variant ofa compound” refers to a moiety that is identical to the compound exceptthat one hydrogen has been removed and replaced with a bond to the restof the chemical structure. As used herein, a “polyvalent variant of acompound” refers to a moiety that is identical to the compound exceptthat more than one hydrogen has been removed and replaced with a bond orbonds to the rest of the chemical structure. In the instance of asupramolecule, the inventive compound is can also be incorporated intothe supramolecule complex without covalent bonds.

Combination with Other Materials

The materials described herein as useful for a particular layer in anorganic light emitting device may be used in combination with a widevariety of other materials present in the device. For example, emissivedopants disclosed herein may be used in conjunction with a wide varietyof hosts, transport layers, blocking layers, injection layers,electrodes and other layers that may be present. The materials describedor referred to below are non-limiting examples of materials that may beuseful in combination with the compounds disclosed herein, and one ofskill in the art can readily consult the literature to identify othermaterials that may be useful in combination.

Conductivity Dopants:

A charge transport layer can be doped with conductivity dopants tosubstantially alter its density of charge carriers, which will in turnalter its conductivity. The conductivity is increased by generatingcharge carriers in the matrix material, and depending on the type ofdopant, a change in the Fermi level of the semiconductor may also beachieved. Hole-transporting layer can be doped by p-type conductivitydopants and n-type conductivity dopants are used in theelectron-transporting layer.

Non-limiting examples of the conductivity dopants that may be used in anOLED in combination with materials disclosed herein are exemplifiedbelow together with references that disclose those materials:EP01617493, EP01968131, EP2020694, EP2684932, 0520050139810,0520070160905, 0520090167167, 052010288362, WO06081780, WO2009003455,WO2009008277, WO2009011327, WO2014009310, 052007252140, 052015060804,0520150123047, and US2012146012.

HIL/HTL:

A hole injecting/transporting material to be used in the presentinvention is not particularly limited, and any compound may be used aslong as the compound is typically used as a hole injecting/transportingmaterial. Examples of the material include, but are not limited to: aphthalocyanine or porphyrin derivative; an aromatic amine derivative; anindolocarbazole derivative; a polymer containing fluorohydrocarbon; apolymer with conductivity dopants; a conducting polymer, such asPEDOT/PSS; a self-assembly monomer derived from compounds such asphosphoric acid and silane derivatives; a metal oxide derivative, suchas MoO_(x); a p-type semiconducting organic compound, such as1,4,5,8,9,12-Hexaazatriphenylenehexacarbonitrile; a metal complex, and across-linkable compounds.

Examples of aromatic amine derivatives used in HIL or HTL include, butnot limit to the following general structures:

Each of Ar¹ to Ar⁹ is selected from the group consisting of aromatichydrocarbon cyclic compounds such as benzene, biphenyl, triphenyl,triphenylene, naphthalene, anthracene, phenalene, phenanthrene,fluorene, pyrene, chrysene, perylene, and azulene; the group consistingof aromatic heterocyclic compounds such as dibenzothiophene,dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran,benzothiophene, benzoselenophene, carbazole, indolocarbazole,pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole,oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole,pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine,oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine,benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline,cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine,pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine,benzofuropyridine, furodipyridine, benzothienopyridine,thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine;and the group consisting of 2 to 10 cyclic structural units which aregroups of the same type or different types selected from the aromatichydrocarbon cyclic group and the aromatic heterocyclic group and arebonded to each other directly or via at least one of oxygen atom,nitrogen atom, sulfur atom, silicon atom, phosphorus atom, boron atom,chain structural unit and the aliphatic cyclic group. Each Ar may beunsubstituted or may be substituted by a substituent selected from thegroup consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl,heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl,cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylicacids, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl,phosphino, and combinations thereof.

In one aspect, Ar¹ to Ar⁹ is independently selected from the groupconsisting of:

wherein k is an integer from 1 to 20; X¹⁰¹ to X¹⁰⁸ is C (including CH)or N; Z¹⁰¹ is NAr¹, O, or S; Ar¹ has the same group defined above.

Examples of metal complexes used in HIL or HTL include, but are notlimited to the following general formula:

wherein Met is a metal, which can have an atomic weight greater than 40;(Y¹⁰¹-Y¹⁰²) is a bidentate ligand, Y¹⁰¹ and Y¹⁰² are independentlyselected from C, N, O, P, and S; L¹⁰¹ is an ancillary ligand; k′ is aninteger value from 1 to the maximum number of ligands that may beattached to the metal; and k′+k″ is the maximum number of ligands thatmay be attached to the metal.

In one aspect, (Y¹⁰¹-Y¹⁰²) is a 2-phenylpyridine derivative. In anotheraspect, (Y¹⁰¹-Y¹⁰²) is a carbene ligand. In another aspect, Met isselected from Ir, Pt, Os, and Zn. In a further aspect, the metal complexhas a smallest oxidation potential in solution vs. Fc⁺/Fc couple lessthan about 0.6 V.

Non-limiting examples of the HIL and HTL materials that may be used inan OLED in combination with materials disclosed herein are exemplifiedbelow together with references that disclose those materials:CN102702075, DE102012005215, EP01624500, EP01698613, EP01806334,EP01930964, EP01972613, EP01997799, EP02011790, EP02055700, EP02055701,EP1725079, EP2085382, EP2660300, EP650955, JP07-073529, JP2005112765,JP2007091719, JP2008021687, JP2014-009196, KR20110088898, KR20130077473,TW201139402, U.S. Ser. No. 06/517,957, US20020158242, US20030162053,US20050123751, US20060182993, US20060240279, US20070145888,US20070181874, US20070278938, US20080014464, US20080091025,US20080106190, US20080124572, US20080145707, US20080220265,US20080233434, US20080303417, US2008107919, US20090115320,US20090167161, US2009066235, US2011007385, US20110163302, US2011240968,US2011278551, US2012205642, US2013241401, US20140117329, US2014183517,U.S. Pat. Nos. 5,061,569, 5,639,914, WO05075451, WO07125714, WO08023550,WO08023759, WO2009145016, WO2010061824, WO2011075644, WO2012177006,WO2013018530, WO2013039073, WO2013087142, WO2013118812, WO2013120577,WO2013157367, WO2013175747, WO2014002873, WO2014015935, WO2014015937,WO2014030872, WO2014030921, WO2014034791, WO2014104514, WO2014157018.

EBL:

An electron blocking layer (EBL) may be used to reduce the number ofelectrons and/or excitons that leave the emissive layer. The presence ofsuch a blocking layer in a device may result in substantially higherefficiencies, and/or longer lifetime, as compared to a similar devicelacking a blocking layer. Also, a blocking layer may be used to confineemission to a desired region of an OLED. In some embodiments, the EBLmaterial has a higher LUMO (closer to the vacuum level) and/or highertriplet energy than the emitter closest to the EBL interface. In someembodiments, the EBL material has a higher LUMO (closer to the vacuumlevel) and/or higher triplet energy than one or more of the hostsclosest to the EBL interface. In one aspect, the compound used in EBLcontains the same molecule or the same functional groups used as one ofthe hosts described below.

Host:

The light emitting layer of the organic EL device of the presentinvention preferably contains at least a metal complex as light emittingmaterial, and may contain a host material using the metal complex as adopant material. Examples of the host material are not particularlylimited, and any metal complexes or organic compounds may be used aslong as the triplet energy of the host is larger than that of thedopant. Any host material may be used with any dopant so long as thetriplet criteria is satisfied.

Examples of metal complexes used as host are preferred to have thefollowing general formula:

wherein Met is a metal; (Y¹⁰³-Y¹⁰⁴)) is a bidentate ligand, Y¹⁰³ andY¹⁰⁴ are independently selected from C, N, O, P, and S; L¹⁰¹ is ananother ligand; k′ is an integer value from 1 to the maximum number ofligands that may be attached to the metal; and k′+k″ is the maximumnumber of ligands that may be attached to the metal.

In one aspect, the metal complexes are:

wherein (O—N) is a bidentate ligand, having metal coordinated to atoms Oand N.

In another aspect, Met is selected from Ir and Pt. In a further aspect,(Y¹⁰³-Y¹⁰⁴) is a carbene ligand.

In one aspect, the host compound contains at least one of the followinggroups selected from the group consisting of aromatic hydrocarbon cycliccompounds such as benzene, biphenyl, triphenyl, triphenylene,tetraphenylene, naphthalene, anthracene, phenalene, phenanthrene,fluorene, pyrene, chrysene, perylene, and azulene; the group consistingof aromatic heterocyclic compounds such as dibenzothiophene,dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran,benzothiophene, benzoselenophene, carbazole, indolocarbazole,pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole,oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole,pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine,oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine,benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline,cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine,pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine,benzofuropyridine, furodipyridine, benzothienopyridine,thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine;and the group consisting of 2 to 10 cyclic structural units which aregroups of the same type or different types selected from the aromatichydrocarbon cyclic group and the aromatic heterocyclic group and arebonded to each other directly or via at least one of oxygen atom,nitrogen atom, sulfur atom, silicon atom, phosphorus atom, boron atom,chain structural unit and the aliphatic cyclic group. Each option withineach group may be unsubstituted or may be substituted by a substituentselected from the group consisting of deuterium, halogen, alkyl,cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy,amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl,heteroaryl, acyl, carboxylic acids, ether, ester, nitrile, isonitrile,sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.

In one aspect, the host compound contains at least one of the followinggroups in the molecule:

wherein R¹⁰¹ is selected from the group consisting of hydrogen,deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl,arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl,heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acids, ether,ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, andcombinations thereof, and when it is aryl or heteroaryl, it has thesimilar definition as Ar's mentioned above. k is an integer from 0 to 20or 1 to 20. X¹⁰¹ to X¹⁰⁸ are independently selected from C (includingCH) or N. Z¹⁰¹ and Z¹⁰² are independently selected from NR¹⁰¹, O, or S.

Non-limiting examples of the host materials that may be used in an OLEDin combination with materials disclosed herein are exemplified belowtogether with references that disclose those materials: EP2034538,EP2034538A, EP2757608, JP2007254297, KR20100079458, KR20120088644,KR20120129733, KR20130115564, TW201329200, US20030175553, US20050238919,US20060280965, US20090017330, US20090030202, US20090167162,US20090302743, US20090309488, US20100012931, US20100084966,US20100187984, US2010187984, US2012075273, US2012126221, US2013009543,US2013105787, US2013175519, US2014001446, US20140183503, US20140225088,US2014034914, U.S. Pat. No. 7,154,114, WO2001039234, WO2004093207,WO2005014551, WO2005089025, WO2006072002, WO2006114966, WO2007063754,WO2008056746, WO2009003898, WO2009021126, WO2009063833, WO2009066778,WO2009066779, WO2009086028, WO2010056066, WO2010107244, WO2011081423,WO2011081431, WO2011086863, WO2012128298, WO2012133644, WO2012133649,WO2013024872, WO2013035275, WO2013081315, WO2013191404, WO2014142472,US20170263869, US20160163995, U.S. Pat. No. 9,466,803,

Additional Emitters:

One or more additional emitter dopants may be used in conjunction withthe compound of the present disclosure. Examples of the additionalemitter dopants are not particularly limited, and any compounds may beused as long as the compounds are typically used as emitter materials.Examples of suitable emitter materials include, but are not limited to,compounds which can produce emissions via phosphorescence, fluorescence,thermally activated delayed fluorescence, i.e., TADF (also referred toas E-type delayed fluorescence), triplet-triplet annihilation, orcombinations of these processes.

Non-limiting examples of the emitter materials that may be used in anOLED in combination with materials disclosed herein are exemplifiedbelow together with references that disclose those materials:CN103694277, CN1696137, EB01238981, EP01239526, EP01961743, EP1239526,EP1244155, EP1642951, EP1647554, EP1841834, EP1841834B, EP2062907,EP2730583, JP2012074444, JP2013110263, JP4478555, KR1020090133652,KR20120032054, KR20130043460, TW201332980, U.S. Ser. No. 06/699,599,U.S. Ser. No. 06/916,554, US20010019782, US20020034656, US20030068526,US20030072964, US20030138657, US20050123788, US20050244673,US2005123791, US2005260449, US20060008670, US20060065890, US20060127696,US20060134459, US20060134462, US20060202194, US20060251923,US20070034863, US20070087321, US20070103060, US20070111026,US20070190359, US20070231600, US2007034863, US2007104979, US2007104980,US2007138437, US2007224450, US2007278936, US20080020237, US20080233410,US20080261076, US20080297033, US200805851, US2008161567, US2008210930,US20090039776, US20090108737, US20090115322, US20090179555,US2009085476, US2009104472, US20100090591, US20100148663, US20100244004,US20100295032, US2010102716, US2010105902, US2010244004, US2010270916,US20110057559, US20110108822, US20110204333, US2011215710, US2011227049,US2011285275, US2012292601, US20130146848, US2013033172, US2013165653,US2013181190, US2013334521, US20140246656, US2014103305, U.S. Pat. Nos.6,303,238, 6,413,656, 6,653,654, 6,670,645, 6,687,266, 6,835,469,6,921,915, 7,279,704, 7,332,232, 7,378,162, 7,534,505, 7,675,228,7,728,137, 7,740,957, 7,759,489, 7,951,947, 8,067,099, 8,592,586,8,871,361, WO06081973, WO06121811, WO07018067, WO07108362, WO07115970,WO07115981, WO08035571, WO2002015645, WO2003040257, WO2005019373,WO2006056418, WO2008054584, WO2008078800, WO2008096609, WO2008101842,WO2009000673, WO2009050281, WO2009100991, WO2010028151, WO2010054731,WO2010086089, WO2010118029, WO2011044988, WO2011051404, WO2011107491,WO2012020327, WO2012163471, WO2013094620, WO2013107487, WO2013174471,WO2014007565, WO2014008982, WO2014023377, WO2014024131, WO2014031977,WO2014038456, WO2014112450.

HBL:

A hole blocking layer (HBL) may be used to reduce the number of holesand/or excitons that leave the emissive layer. The presence of such ablocking layer in a device may result in substantially higherefficiencies and/or longer lifetime as compared to a similar devicelacking a blocking layer. Also, a blocking layer may be used to confineemission to a desired region of an OLED. In some embodiments, the HBLmaterial has a lower HOMO (further from the vacuum level) and/or highertriplet energy than the emitter closest to the HBL interface. In someembodiments, the HBL material has a lower HOMO (further from the vacuumlevel) and/or higher triplet energy than one or more of the hostsclosest to the HBL interface.

In one aspect, compound used in HBL contains the same molecule or thesame functional groups used as host described above.

In another aspect, compound used in HBL contains at least one of thefollowing groups in the molecule:

wherein k is an integer from 1 to 20; L¹⁰¹ is an another ligand, k′ isan integer from 1 to 3.ETL:

Electron transport layer (ETL) may include a material capable oftransporting electrons. Electron transport layer may be intrinsic(undoped), or doped. Doping may be used to enhance conductivity.Examples of the ETL material are not particularly limited, and any metalcomplexes or organic compounds may be used as long as they are typicallyused to transport electrons.

In one aspect, compound used in ETL contains at least one of thefollowing groups in the molecule:

wherein R¹⁰¹ is selected from the group consisting of hydrogen,deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl,arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl,heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acids, ether,ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, andcombinations thereof, when it is aryl or heteroaryl, it has the similardefinition as Ar's mentioned above. Ar¹ to Ar³ has the similardefinition as Ar's mentioned above. k is an integer from 1 to 20. X¹⁰¹to X¹⁰⁸ is selected from C (including CH) or N.

In another aspect, the metal complexes used in ETL contains, but notlimit to the following general formula:

wherein (O—N) or (N—N) is a bidentate ligand, having metal coordinatedto atoms O, N or N, N; L¹⁰¹ is another ligand; k′ is an integer valuefrom 1 to the maximum number of ligands that may be attached to themetal.

Non-limiting examples of the ETL materials that may be used in an OLEDin combination with materials disclosed herein are exemplified belowtogether with references that disclose those materials: CN103508940,EP01602648, EP01734038, EP01956007, JP2004-022334, JP2005149918,JP2005-268199, KR0117693, KR20130108183, US20040036077, US20070104977,US2007018155, US20090101870, US20090115316, US20090140637,US20090179554, US2009218940, US2010108990, US2011156017, US2011210320,US2012193612, US2012214993, US2014014925, US2014014927, US20140284580,U.S. Pat. Nos. 6,656,612, 8,415,031, WO2003060956, WO2007111263,WO2009148269, WO2010067894, WO2010072300, WO2011074770, WO2011105373,WO2013079217, WO2013145667, WO2013180376, WO2014104499, WO2014104535,

Charge Generation Layer (CGL)

In tandem or stacked OLEDs, the CGL plays an essential role in theperformance, which is composed of an n-doped layer and a p-doped layerfor injection of electrons and holes, respectively. Electrons and holesare supplied from the CGL and electrodes. The consumed electrons andholes in the CGL are refilled by the electrons and holes injected fromthe cathode and anode, respectively; then, the bipolar currents reach asteady state gradually. Typical CGL materials include n and pconductivity dopants used in the transport layers.

In any above-mentioned compounds used in each layer of the OLED device,the hydrogen atoms can be partially or fully deuterated. Thus, anyspecifically listed substituent, such as, without limitation, methyl,phenyl, pyridyl, etc. may be undeuterated, partially deuterated, andfully deuterated versions thereof. Similarly, classes of substituentssuch as, without limitation, alkyl, aryl, cycloalkyl, heteroaryl, etc.also may be undeuterated, partially deuterated, and fully deuteratedversions thereof.

EXPERIMENTALS Synthesis of the Inventive Example Compound 1 with Formulaof Ir(L_(A66-1))₂L_(C17)

Solution of1-(4-(tert-butyl)naphthalen-2-yl)-8-isobutylbenzo[4,5]thieno[2,3-c]pyri-dine(8.43 g, 19.9 mmol, 2.1 equiv) in 2-ethoxyethanol (125 mL) and deionizedultra-filtered (DIUF) water (80 mL) was sparged with nitrogen for 10minutes. Iridium chloride(III) hydrate (3.019 g, 9.54 mmol, 1.0 equiv)was added and the reaction mixture heated at 95° C. for 18 hours. Thesolution was cooled to 50° C., the solids were filtered, washed withDIUF water (125 mL) and methanol (125 mL) then air-dried to give solventwetdi-μ-chloro-tetrakis-[(1-(4-(tert-butyl)naphthalen-2-yl)-1′-yl)-8-iso-butylbenzo[4,5]thieno[2,3-c]pyridin-6-yl]diiridium(III).

Next, to a solution ofdi-μ-chloro-tetrakis-[(1-(4-(tert-butyl)naphthalen-2-yl)-1′-yl)-8-isobutylbenzo[4,5]thieno[2,3-c]pyridin-6-yl]iridium(III)(10.23 g, 4.77 mmol, 1.0 equiv) in 2-ethoxyethanol (150 mL) was added,via syringe, 3,7-di-ethylnonane-4,6-dione (5.516 g, 26.0 mmol, 5.45equiv) and the reaction mixture sparged with nitrogen for 15 minutes.Powdered potassium carbonate (5.317 g, 38.5 mmol, 8.07 equiv) was addedand the reaction mixture stirred at room temperature for 72 hours. DIUFwater (150 mL) was added and the mixture stirred for 30 minutes. Thesuspension was filtered, the solid washed with DIUF water (250 mL) andmethanol (200 mL) then air-dried. The crude red solid (16.6 g) waschromatographed on silica gel (843 g) layered with basic alumina (468g), eluting with 40% dichloromethane in hexanes to givebis[(1-(4-(tert-butyl)naphthalen-2-yl)-1′-yl)-8-isobutylbenzo[4,5]thieno[2,3-c]pyridin-2-yl]-(3,7-diethylnonane-4,6-dionato-k₂O,O′)iridium(III).

Synthesis of Inventive Example Compound 2

8-Isobutyl-1-(naphthalen-2-yl)benzo[4,5]thieno[2,3-c]pyridine (2.40 g,6.53 mmol, 2.2 equiv) and iridium(III) chloride tetrahydrate (1.1 g,2.97 mmol, 1.0 equiv) were charged to 40 mL reaction vial.2-Ethoxyethanol (15 mL) and DIUF water (5 mL) were added and thereaction mixture stirred at 90° C. for about 60 hours. ¹H-NMR analysisindicated complete consumption of the starting ligand. The mixture wascooled to room temperature and diluted with DIUF water (5 mL). Thesolids were filtered and washed with methanol (20 mL) to givedi-μ-chloro-tetrakis[1-(naphthalen-2-yl)-3′-yl)-8-isobutyl-benzo[4,5]thieno[2,3-c]pyridin-2-yl)]-diiridium(III)(1.42 g, 52% yield) as an orange solid.

A mixture of 3,7-diethylnonane-4,6-dione (1.180 g, 5.56 mmol, 8 equiv),crude di-μ-chloro-tetrakis[1-(naphthalenyl)-3′-yl)-8-isobutyl-benzo[4,5]thieno[2,3-c]pyridin-2-yl)]-diiridium(III)(1.39 g, 0.722 mmol, 1.0 equiv), dichloromethane (1 mL) and methanol (25mL) were charged to a 40 mL vial. Powdered potassium carbonate (1.152 g,8.34 mmol, 12 equiv) was added and the mixture sparged with nitrogen for5 minutes. After heating at 45° C. overnight, the reaction was cooled toroom temperature and diluted with DIUF water (50 mL). After stirring for10 minutes, the red-orange solid was filtered, washed with water (20mL), then methanol (100 mL) and dried under vacuum, The solid wasdissolved in dichloromethane (200 mL) and thy-loaded onto Celite (50 g).The product was chromatographed on basic alumina to affordbis[(1-(naphthalen-2-yl)-3′-yl)-8-isobutyl-benzo[4,5]thieno[2,3-c]pyridin-2-yl)]-(3,7-diethyl-4,6-nonanedionato-κ₂O,O′)iridium(III) (0.705 g, 97.2% purity, 43% yield) as a red-orange solid.

Synthesis of Comparative Example 1 Compound

A suspension of8-isobutyl-1-(naphthalen-1-yl)benzo[4,5]thieno[2,3-c]pyridine (1.695 g,4.61 mmol, 2.0 equiv) in 2-ethoxyethanol (12 mL) and DIUF water (4 mL)was sparged with nitrogen for 10 minutes. Iridium(III) chloride hydrate(0.73 g, 2.31 mmol, 1.0 equiv) was added, and the reaction mixtureheated at 100° C. for 18 hours. The reaction was stopped and cooled toroom temperature. The resulting red solid was filtered and washed withmethanol (3×5 mL) to give the crude presumed intermediatedi-μ-chloro-tetrakis[1-(naphthalen-1-yl)-2′-yl)-8-isobutyl-benzo[4,5]thieno[2,3-c]pyridin-1-yl)]-diiridium(III)(est. 1.153 mmol, wet) as a red solid.

Next, crudedi-μ-chloro-tetrakis[1-(naphthalen-1-yl)-2′-yl)-8-isobutyl-benzo[4,5]thieno[2,3-c]pyridin-1-yl)]-diiridium(III)(est. 1.153 mmol, 1.0 equiv) was suspended in methanol (12 mL) anddichloromethane (1 mL). 3,7-Diethylnonane-4,6-dione (0.98 g, 4.61 mmol,4.0 equiv) and powdered potassium carbonate (0.96 g, 6.92 mmol, 6.0equiv) were added and the reaction mixture heated at 50° C. for 2 hoursto form a new red suspension. The reaction was cooled to roomtemperature and diluted with water (10 mL). The solid was filtered andwashed with water (2×3 mL) and methanol (3×1 mL). The red solid waspurified on silica gel column eluted with a gradient of 0 to 50%dichloromethane in heptanes to givebis[(1-(naphthalen-1-yl)-2′-yl)-8-isobutyl-benzo[4,5]thieno[2,3-c]pyridin-1-yl)]-(3,7-diethyl-4,6-nonanedionato-k₂O,O′)iridium(III).

A photoluminescence (PL) spectra of compounds of the Inventive ExampleI, Inventive Example 2, and the Comparative Example 1 were taken in2-methylTHF solution at room temperature and the data are shown in theplot in FIG. 3 . The PL intensities are normalized to the maximum of thefirst emission peaks. Both the Inventive Example 1 and the ComparativeExample 1 show saturated red color. Compared to the Comparative Example1, the Inventive Example 1 shows much narrower emission. It can be seenthat the intensity of the second PL peak of the Inventive Example 1 islower than that of the Comparative Example 1. The saturated emissioncolor, narrower emission spectrum, more specifically the lowercontribution from the second emission peak offers improved deviceperformance, such as high electroluminescence efficiency and lower powerconsumption.

It is understood that the various embodiments described herein are byway of example only, and are not intended to limit the scope of theinvention. For example, many of the materials and structures describedherein may be substituted with other materials and structures withoutdeviating from the spirit of the invention. The present invention asclaimed may therefore include variations from the particular examplesand preferred embodiments described herein, as will be apparent to oneof skill in the art. It is understood that various theories as to whythe invention works are not intended to be limiting.

We claim:
 1. A compound comprising a ligand L_(A) of Formula I:

wherein Ring B represents a five- or six-membered aromatic ring; whereinR³ represents from none to the maximum number of substitutions; whereinX¹, X², X³, and X⁴ are each independently a CR or N; wherein at leasttwo adjacent ones of X¹, X², X³, and X⁴ are CR and fused into afive-membered aromatic ring; wherein R¹ is CR¹¹R¹²R¹³ or joined with R²to form into a ring; wherein R, R¹, R², R³, R¹¹, R¹², and R¹³ are eachindependently selected from the group consisting of hydrogen, deuterium,halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy,amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl,heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile,sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;wherein any two substituents among R, R¹, R², and R³, are optionallyjoined to form into an aromatic ring; wherein two substituents amongR¹¹, R¹², and R¹³ are optionally joined to form into a ring; whereinL_(A) is coordinated to a metal M; wherein L_(A) is optionally linkedwith other ligands to comprise a tridentate, tetradentate, pentadentate,or hexadentate ligand; and wherein M is optionally coordinated to otherligands.
 2. The compound of claim 1, wherein M is selected from thegroup consisting of Ir, Rh, Re, Ru, Os, Pt, Au, and Cu.
 3. The compoundof claim 1, wherein M is Ir or Pt.
 4. The compound of claim 1, whereintwo of R¹¹, R¹², and R¹³ are joined to form a ring; or at least two ofR¹¹, R¹², and R¹³ are each independently selected from the groupconsisting of alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy,aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl,aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile,isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, partially or fullydeuterated variants thereof partially or fully fluorinated variantsthereof, and combinations thereof.
 5. The compound of claim 1, whereinR¹ is tert-butyl or substituted tert-butyl.
 6. The compound of claim 1,wherein Ring B is phenyl.
 7. The compound of claim 1, wherein the ligandL_(A) is selected from the group consisting of:

wherein X is O or S; wherein R¹, R², R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹,R¹², R¹³, R¹⁴, R¹⁵, R¹⁶, R¹⁷, R¹⁸, and R¹⁹ are each independentlyselected from the group consisting of hydrogen, deuterium, halogen,alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino,silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl,acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl,sulfinyl, sulfonyl, phosphino, and combinations thereof; wherein any twosubstituents are optionally joined to form into a ring.
 8. The compoundof claim 1, wherein the ligand L_(A) is selected from the groupconsisting of: ligands XVIII-L_(Ai-O) that are based on a structure ofFormula XVIII

where X is O, and ligands XVIII-L_(Ai-S) that are based on a structureof Formula XVIII, where X is S; ligands XIX-L_(Ai-O) that are based on astructure of Formula XIX

where X is O, and ligands XIX-L_(Ai-S) that are based on a structure ofFormula XIX, where X is S; ligands XX-L_(Ai-O) that are based on astructure of Formula XX

where X is O, and ligands XX-L_(Ai-S) that are based on a structure ofFormula XX, where X is S; ligands XXI-L_(Ai-O) that are based on astructure of Formula XXI

where X is O, and ligands XXI-L_(Ai-S) that are based on a structure ofFormula XXI, where X is S; ligands XXII-L_(Ai-O) that are based on astructure of Formula XXII

where X is O, and ligands XXII-L_(Ai-S) that are based on a structure ofFormula XXII, where X is S; ligands XXIII-L_(Ai-O) that are based on astructure of Formula XXIII

where X is O, and ligands XXIII-L_(Ai-S) that are based on a structureof Formula XXIII, where X is S; ligands XXIV-L_(Ai-O) that are based ona structure of Formula XXIV

where X is O, and ligands XXIV-L_(Ai-S) that are based on a structure ofFormula XXIV, where X is S; ligands XXV-L_(Ai-O) that are based on astructure of Formula XXV

where X is O, and ligands XXV-L_(Ai-S) that are based on a structure ofFormula XXV, where X is S; ligands XXVI-L_(Ai-O) that are based on astructure of Formula XXVI

where X is O, and ligands XXVI-L_(Ai-S) that are based on a structure ofFormula XXVI, where X is S; ligands XXVII-L_(Ai-O) that are based on astructure of Formula XXVII

where X is O, and ligands XXVII-L_(Ai-S) that are based on a structureof Formula XXVII, where X is S; ligands XXVIII-L_(Ai-O) that are basedon a structure of Formula XXVII

where X is O, and ligands XXVIII-L_(Ai-S) that are based on a structureof Formula XXVIII, where X is S; ligands XXIX-L_(Ai-O) that are based ona structure of Formula XXIX

where X is O, and ligands XXIX-L_(Ai-S) that are based on a structure ofFormula XXIX, where X is S; ligands XXX-L_(Ai-O) that are based on astructure of Formula XXX

where X is O, and ligands XXX-L_(Ai-S) that are based on a structure ofFormula XXX, where X is S; ligands XXXI-L_(Ai-O) that are based on astructure of Formula XXXI

where X is O, and ligands XXXI-L_(Ai-S) that are based on a structure ofFormula XXXI, where X is S; ligands XXXII-L_(Ai-O) that are based on astructure of Formula XXXII

where X is O, and ligands XXXII-L_(Ai-S) that are based on a structureof Formula XXXII, where X is S; ligands XXXIII-L_(Ai-O) that are basedon a structure of Formula XXXIII

where X is O, and ligands XXXIII-L_(Ai-S) that are based on a structureof Formula XXXIII, where X is S; ligands XXXIV-L_(Ai-O) that are basedon a structure of Formula XXXIV

where X is O, and ligands XXXIV-L_(Ai-S) that are based on a structureof Formula XXXIV, where X is S; ligands XXXV-L_(Ai-O) that are based ona structure of Formula XXXV

where X is O, and ligands XXXV-L_(Ai-S) that are based on a structure ofFormula XXXV, where X is S; ligands XXXVI-L_(Ai-O) that are based on astructure of Formula XXXVI

where X is O, and ligands XXXVI-L_(Ai-S) that are based on a structureof Formula XXXVI, where X is S; ligands XXXVII-L_(Ai-O) that are basedon a structure of Formula XXXVII

where X is O, and ligands XXXVII-L_(Ai-S) that are based on a structureof Formula XXXVII, where X is S; ligands XXXVIII-L_(Ai-O) that are basedon a structure of Formula XXXVIII

where X is O, and ligands XXXVIII-L_(Ai-S) that are based on a structureof Formula XXXVIII, where X is S; ligands XXXIX-L_(Ai-O) that are basedon a structure of Formula XXXIX

where X is O, and ligands XXXIX-L_(Ai-S) that are based on a structureof Formula XXXIX, where X is S; ligands XL-L_(Ai-O) that are based on astructure of Formula XL

where X is O, and ligands XL-L_(Ai-S) that are based on a structure ofFormula XL, where X is S; ligands XLI-L_(Ai-O) that are based on astructure of Formula XLI

where X is O, and ligands XLI-L_(Ai-S) that are based on a structure ofFormula XLI, where X is S; ligands XLII-L_(Ai-O) that are based on astructure of Formula XLII

where X is O, and ligands XLII-L_(Ai-S) that are based on a structure ofFormula XLII, where X is S; ligands XLIII-L_(Ai-O) that are based on astructure of Formula XLIII

where X is O, and ligands XLIII-L_(Ai-S) that are based on a structureof Formula XLIII, where X is S; ligands XLIV-L_(Ai-O) that are based ona structure of Formula XLIV

where X is O, and ligands XLIV-L_(Ai-S) that are based on a structure ofFormula XLIV, where X is S; wherein i is an integer from 1171 to 1584and for each i, R¹, R¹¹, and R¹² in the formulas XVIII through XLIV aredefined as follows: L_(Ai) R¹ R¹¹ R¹² L_(A1171) R_(B3) H H L_(A1172)R_(B3) R_(B1) H L_(A1173) R_(B3) R_(B3) H L_(A1174) R_(B3) R_(B4) HL_(A1175) R_(B3) R_(B5) H L_(A1176) R_(B3) R_(B6) H L_(A1177) R_(B3)R_(B7) H L_(A1178) R_(B3) R_(B24) H L_(A1179) R_(B3) R_(B25) H L_(A1180)R_(B3) R_(A3) H L_(A1181) R_(B3) R_(A34) H L_(A1182) R_(B3) R_(A44) HL_(A1183) R_(B3) R_(A52) H L_(A1184) R_(B3) R_(A53) H L_(A1185) R_(B3)R_(A54) H L_(A1186) R_(B3) R_(C3) H L_(A1187) R_(B3) R_(C4) H L_(A1188)R_(B3) R_(C8) H L_(A1189) R_(B3) H R_(B1) L_(A1190) R_(B3) H R_(B3)L_(A1191) R_(B3) H R_(B4) L_(A1192) R_(B3) H R_(B5) L_(A1193) R_(B3) HR_(B6) L_(A1194) R_(B3) H R_(B7) L_(A1195) R_(B3) H R_(B24) L_(A1196)R_(B3) H R_(B25) L_(A1197) R_(B3) H R_(A3) L_(A1198) R_(B3) H R_(A34)L_(A1199) R_(B3) H R_(A44) L_(A1200) R_(B3) H R_(A52) L_(A1201) R_(B3) HR_(A53) L_(A1202) R_(B3) H R_(A54) L_(A1203) R_(B3) H R_(C3) L_(A1204)R_(B3) H R_(C4) L_(A1205) R_(B3) H R_(C8) L_(A1206) R_(B3) R_(B1) R_(B1)L_(A1207) R_(B3) R_(B3) R_(B1) L_(A1208) R_(B3) R_(B4) R_(B1) L_(A1209)R_(B3) R_(B5) R_(B1) L_(A1210) R_(B3) R_(B6) R_(B1) L_(A1211) R_(B3)R_(B7) R_(B1) L_(A1212) R_(B3) R_(B24) R_(B1) L_(A1213) R_(B3) R_(B25)R_(B1) L_(A1214) R_(B3) R_(A3) R_(B1) L_(A1215) R_(B3) R_(A34) R_(B1)L_(A1216) R_(B3) R_(A44) R_(B1) L_(A1217) R_(B3) R_(A52) R_(B1)L_(A1218) R_(B3) R_(A53) R_(B1) L_(A1219) R_(B3) R_(A54) R_(B1)L_(A1220) R_(B3) R_(C3) R_(B1) L_(A1221) R_(B3) R_(C4) R_(B1) L_(A1222)R_(B3) R_(C8) R_(B1) L_(A1223) R_(B3) R_(B1) R_(B1) L_(A1224) R_(B3)R_(B1) R_(B3) L_(A1225) R_(B3) R_(B1) R_(B4) L_(A1226) R_(B3) R_(B1)R_(B5) L_(A1227) R_(B3) R_(B1) R_(B6) L_(A1228) R_(B3) R_(B1) R_(B7)L_(A1229) R_(B3) R_(B1) R_(B24) L_(A1230) R_(B3) R_(B1) R_(B25)L_(A1231) R_(B3) R_(B1) R_(A3) L_(A1232) R_(B3) R_(B1) R_(A34) L_(A1233)R_(B3) R_(B1) R_(A44) L_(A1234) R_(B3) R_(B1) R_(A52) L_(A1235) R_(B3)R_(B1) R_(A53) L_(A1236) R_(B3) R_(B1) R_(A54) L_(A1237) R_(B3) R_(B1)R_(C3) L_(A1238) R_(B3) R_(B1) R_(C4) L_(A1239) R_(B3) R_(B1) R_(C8)L_(A1240) R_(B6) H H L_(A1241) R_(B6) R_(B1) H L_(A1242) R_(B6) R_(B3) HL_(A1243) R_(B6) R_(B4) H L_(A1244) R_(B6) R_(B5) H L_(A1245) R_(B6)R_(B6) H L_(A1246) R_(B6) R_(B7) H L_(A1247) R_(B6) R_(B24) H L_(A1248)R_(B6) R_(B25) H L_(A1249) R_(B6) R_(A3) H L_(A1250) R_(B6) R_(A34) HL_(A1251) R_(B6) R_(A44) H L_(A1252) R_(B6) R_(A52) H L_(A1253) R_(B6)R_(A53) H L_(A1254) R_(B6) R_(A54) H L_(A1255) R_(B6) R_(C3) H L_(A1256)R_(B6) R_(C4) H L_(A1257) R_(B6) R_(C8) H L_(A1258) R_(B6) H R_(B1)L_(A1259) R_(B6) H R_(B3) L_(A1260) R_(B6) H R_(B4) L_(A1261) R_(B6) HR_(B5) L_(A1262) R_(B6) H R_(B6) L_(A1263) R_(B6) H R_(B7) L_(A1264)R_(B6) H R_(B24) L_(A1265) R_(B6) H R_(B25) L_(A1266) R_(B6) H R_(A3)L_(A1267) R_(B6) H R_(A34) L_(A1268) R_(B6) H R_(A44) L_(A1269) R_(B6) HR_(A52) L_(A1270) R_(B6) H R_(A53) L_(A1271) R_(B6) H R_(A54) L_(A1272)R_(B6) H R_(C3) L_(A1273) R_(B6) H R_(C4) L_(A1274) R_(B6) H R_(C8)L_(A1275) R_(B6) R_(B1) R_(B1) L_(A1276) R_(B6) R_(B3) R_(B1) L_(A1277)R_(B6) R_(B4) R_(B1) L_(A1278) R_(B6) R_(B5) R_(B1) L_(A1279) R_(B6)R_(B6) R_(B1) L_(A1280) R_(B6) R_(B7) R_(B1) L_(A1281) R_(B6) R_(B24)R_(B1) L_(A1282) R_(B6) R_(B25) R_(B1) L_(A1283) R_(B6) R_(A3) R_(B1)L_(A1284) R_(B6) R_(A34) R_(B1) L_(A1285) R_(B6) R_(A44) R_(B1)L_(A1286) R_(B6) R_(A52) R_(B1) L_(A1287) R_(B6) R_(A53) R_(B1)L_(A1288) R_(B6) R_(A54) R_(B1) L_(A1289) R_(B6) R_(C3) R_(B1) L_(A1290)R_(B6) R_(C4) R_(B1) L_(A1291) R_(B6) R_(C8) R_(B1) L_(A1292) R_(B6)R_(B1) R_(B1) L_(A1293) R_(B6) R_(B1) R_(B3) L_(A1294) R_(B6) R_(B1)R_(B4) L_(A1295) R_(B6) R_(B1) R_(B5) L_(A1296) R_(B6) R_(B1) R_(B6)L_(A1297) R_(B6) R_(B1) R_(B7) L_(A1298) R_(B6) R_(B1) R_(B24) L_(A1299)R_(B6) R_(B1) R_(B25) L_(A1300) R_(B6) R_(B1) R_(A3) L_(A1301) R_(B6)R_(B1) R_(A34) L_(A1302) R_(B6) R_(B1) R_(A44) L_(A1303) R_(B6) R_(B1)R_(A52) L_(A1304) R_(B6) R_(B1) R_(A53) L_(A1305) R_(B6) R_(B1) R_(A54)L_(A1306) R_(B6) R_(B1) R_(C3) L_(A1307) R_(B6) R_(B1) R_(C4) L_(A1308)R_(B6) R_(B1) R_(C8) L_(A1309) R_(B7) H H L_(A1310) R_(B7) R_(B1) HL_(A1311) R_(B7) R_(B3) H L_(A1312) R_(B7) R_(B4) H L_(A1313) R_(B7)R_(B5) H L_(A1314) R_(B7) R_(B6) H L_(A1315) R_(B7) R_(B7) H L_(A1316)R_(B7) R_(B24) H L_(A1317) R_(B7) R_(B25) H L_(A1318) R_(B7) R_(A3) HL_(A1319) R_(B7) R_(A34) H L_(A1320) R_(B7) R_(A44) H L_(A1321) R_(B7)R_(A52) H L_(A1322) R_(B7) R_(A53) H L_(A1323) R_(B7) R_(A54) HL_(A1324) R_(B7) R_(C3) H L_(A1325) R_(B7) R_(C4) H L_(A1326) R_(B7)R_(C8) H L_(A1327) R_(B7) H R_(B1) L_(A1328) R_(B7) H R_(B3) L_(A1329)R_(B7) H R_(B4) L_(A1330) R_(B7) H R_(B5) L_(A1331) R_(B7) H R_(B6)L_(A1332) R_(B7) H R_(B7) L_(A1333) R_(B7) H R_(B24) L_(A1334) R_(B7) HR_(B25) L_(A1335) R_(B7) H R_(A3) L_(A1336) R_(B7) H R_(A34) L_(A1337)R_(B7) H R_(A44) L_(A1338) R_(B7) H R_(A52) L_(A1339) R_(B7) H R_(A53)L_(A1340) R_(B7) H R_(A54) L_(A1341) R_(B7) H R_(C3) L_(A1342) R_(B7) HR_(C4) L_(A1343) R_(B7) H R_(C8) L_(A1344) R_(B7) R_(B1) R_(B1)L_(A1345) R_(B7) R_(B3) R_(B1) L_(A1346) R_(B7) R_(B4) R_(B1) L_(A1347)R_(B7) R_(B5) R_(B1) L_(A1348) R_(B7) R_(B6) R_(B1) L_(A1349) R_(B7)R_(B7) R_(B1) L_(A1350) R_(B7) R_(B24) R_(B1) L_(A1351) R_(B7) R_(B25)R_(B1) L_(A1352) R_(B7) R_(A3) R_(B1) L_(A1353) R_(B7) R_(A34) R_(B1)L_(A1354) R_(B7) R_(A44) R_(B1) L_(A1355) R_(B7) R_(A52) R_(B1)L_(A1356) R_(B7) R_(A53) R_(B1) L_(A1357) R_(B7) R_(A54) R_(B1)L_(A1358) R_(B7) R_(C3) R_(B1) L_(A1359) R_(B7) R_(C4) R_(B1) L_(A1360)R_(B7) R_(C8) R_(B1) L_(A1361) R_(B7) R_(B1) R_(B1) L_(A1362) R_(B7)R_(B1) R_(B3) L_(A1363) R_(B7) R_(B1) R_(B4) L_(A1364) R_(B7) R_(B1)R_(B5) L_(A1365) R_(B7) R_(B1) R_(B6) L_(A1366) R_(B7) R_(B1) R_(B7)L_(A1367) R_(B7) R_(B1) R_(B24) L_(A1368) R_(B7) R_(B1) R_(A25)L_(A1369) R_(B7) R_(B1) R_(A3) L_(A1370) R_(B7) R_(B1) R_(A34) L_(A1371)R_(B7) R_(B1) R_(A44) L_(A1372) R_(B7) R_(B1) R_(A52) L_(A1373) R_(B7)R_(B1) R_(A53) L_(A1374) R_(B7) R_(B1) R_(C54) L_(A1375) R_(B7) R_(B1)R_(C3) L_(A1376) R_(B7) R_(B1) R_(C4) L_(A1377) R_(B7) R_(B1) R_(C8)L_(A1378) R_(B9) H H L_(A1379) R_(B9) R_(B1) H L_(A1380) R_(B9) R_(B3) HL_(A1381) R_(B9) R_(B4) H L_(A1382) R_(B9) R_(B5) H L_(A1383) R_(B9)R_(B6) H L_(A1384) R_(B9) R_(B7) H L_(A1385) R_(B9) R_(B24) H L_(A1386)R_(B9) R_(B25) H L_(A1387) R_(B9) R_(A3) H L_(A1388) R_(B9) R_(A34) HL_(A1389) R_(B9) R_(A44) H L_(A1390) R_(B9) R_(A52) H L_(A1391) R_(B9)R_(A53) H L_(A1392) R_(B9) R_(A54) H L_(A1393) R_(B9) R_(C3) H L_(A1394)R_(B9) R_(C4) H L_(A1395) R_(B9) R_(C8) H L_(A1396) R_(B9) H R_(B1)L_(A1397) R_(B9) H R_(B3) L_(A1398) R_(B9) H R_(B4) L_(A1399) R_(B9) HR_(B5) L_(A1400) R_(B9) H R_(B6) L_(A1401) R_(B9) H R_(B7) L_(A1402)R_(B9) H R_(B24) L_(A1403) R_(B9) H R_(B25) L_(A1404) R_(B9) H R_(A3)L_(A1405) R_(B9) H R_(A34) L_(A1406) R_(B9) H R_(A44) L_(A1407) R_(B9) HR_(A52) L_(A1408) R_(B9) H R_(A53) L_(A1409) R_(B9) H R_(A54) L_(A1410)R_(B9) H R_(C3) L_(A1411) R_(B9) H R_(C4) L_(A1412) R_(B9) H R_(C8)L_(A1413) R_(B9) R_(B1) R_(B1) L_(A1414) R_(B9) R_(B3) R_(B1) L_(A1415)R_(B9) R_(B4) R_(B1) L_(A1416) R_(B9) R_(B5) R_(B1) L_(A1417) R_(B9)R_(B6) R_(B1) L_(A1418) R_(B9) R_(B7) R_(B1) L_(A1419) R_(B9) R_(B24)R_(B1) L_(A1420) R_(B9) R_(B25) R_(B1) L_(A1421) R_(B9) R_(A3) R_(B1)L_(A1422) R_(B9) R_(A34) R_(B1) L_(A1423) R_(B9) R_(A44) R_(B1)L_(A1424) R_(B9) R_(A52) R_(B1) L_(A1425) R_(B9) R_(A53) R_(B1)L_(A1426) R_(B9) R_(A54) R_(B1) L_(A1427) R_(B9) R_(C3) R_(B1) L_(A1428)R_(B9) R_(C4) R_(B1) L_(A1429) R_(B9) R_(C8) R_(B1) L_(A1430) R_(B9)R_(B1) R_(B1) L_(A1431) R_(B9) R_(B1) R_(B3) L_(A1432) R_(B9) R_(B1)R_(B4) L_(A1433) R_(B9) R_(B1) R_(B5) L_(A1434) R_(B9) R_(B1) R_(B6)L_(A1435) R_(B9) R_(B1) R_(B7) L_(A1436) R_(B9) R_(B1) R_(B24) L_(A1437)R_(B9) R_(B1) R_(B25) L_(A1438) R_(B9) R_(B1) R_(A3) L_(A1439) R_(B9)R_(B1) R_(A34) L_(A1440) R_(B9) R_(B1) R_(A44) L_(A1441) R_(B9) R_(B1)R_(A52) L_(A1442) R_(B9) R_(B1) R_(A53) L_(A1443) R_(B9) R_(B1) R_(A54)L_(A1444) R_(B9) R_(B1) R_(C3) L_(A1445) R_(B9) R_(B1) R_(C4) L_(A1446)R_(B9) R_(B1) R_(C8) L_(A1447) R_(B15) H H L_(A1448) R_(B15) R_(B1) HL_(A1449) R_(B15) R_(B3) H L_(A1450) R_(B15) R_(B4) H L_(A1451) R_(B15)R_(B5) H L_(A1452) R_(B15) R_(B6) H L_(A1453) R_(B15) R_(B7) H L_(A1454)R_(B15) R_(B24) H L_(A1455) R_(B15) R_(B25) H L_(A1456) R_(B15) R_(A3) HL_(A1457) R_(B15) R_(A34) H L_(A1458) R_(B15) R_(A44) H L_(A1459)R_(B15) R_(A52) H L_(A1460) R_(B15) R_(A53) H L_(A1461) R_(B15) R_(A54)H L_(A1462) R_(B15) R_(C3) H L_(A1463) R_(B15) R_(C4) H L_(A1464)R_(B15) R_(C8) H L_(A1465) R_(B15) H R_(B1) L_(A1466) R_(B15) H R_(B3)L_(A1467) R_(B15) H R_(B4) L_(A1468) R_(B15) H R_(B5) L_(A1469) R_(B15)H R_(B6) L_(A1470) R_(B15) H R_(B7) L_(A1471) R_(B15) H R_(B24)L_(A1472) R_(B15) H R_(B25) L_(A1473) R_(B15) H R_(A3) L_(A1474) R_(B15)H R_(A34) L_(A1475) R_(B15) H R_(A44) L_(A1476) R_(B15) H R_(A52)L_(A1477) R_(B15) H R_(A53) L_(A1478) R_(B15) H R_(A54) L_(A1479)R_(B15) H R_(C3) L_(A1480) R_(B15) H R_(C4) L_(A1481) R_(B15) H R_(C8)L_(A1482) R_(B15) R_(B1) R_(B1) L_(A1483) R_(B15) R_(B3) R_(B1)L_(A1484) R_(B15) R_(B4) R_(B1) L_(A1485) R_(B15) R_(B5) R_(B1)L_(A1486) R_(B15) R_(B6) R_(B1) L_(A1487) R_(B15) R_(B7) R_(B1)L_(A1488) R_(B15) R_(B24) R_(B1) L_(A1489) R_(B15) R_(B25) R_(B1)L_(A1490) R_(B15) R_(A3) R_(B1) L_(A1491) R_(B15) R_(A34) R_(B1)L_(A1492) R_(B15) R_(A44) R_(B1) L_(A1493) R_(B15) R_(A52) R_(B1)L_(A1494) R_(B15) R_(A53) R_(B1) L_(A1495) R_(B15) R_(A54) R_(B1)L_(A1496) R_(B15) R_(C3) R_(B1) L_(A1497) R_(B15) R_(C4) R_(B1)L_(A1498) R_(B15) R_(C8) R_(B1) L_(A1499) R_(B15) R_(B1) R_(B1)L_(A1500) R_(B15) R_(B1) R_(B3) L_(A1501) R_(B15) R_(B1) R_(B4)L_(A1502) R_(B15) R_(B1) R_(B5) L_(A1503) R_(B15) R_(B1) R_(B6)L_(A1504) R_(B15) R_(B1) R_(B7) L_(A1505) R_(B15) R_(B1) R_(B24)L_(A1506) R_(B15) R_(B1) R_(B25) L_(A1507) R_(B15) R_(B1) R_(A3)L_(A1508) R_(B15) R_(B1) R_(A34) L_(A1509) R_(B15) R_(B1) R_(A44)L_(A1510) R_(B15) R_(B1) R_(A52) L_(A1511) R_(B15) R_(B1) R_(A53)L_(A1512) R_(B15) R_(B1) R_(A54) L_(A1513) R_(B15) R_(B1) R_(C3)L_(A1514) R_(B15) R_(B1) R_(C4) L_(A1515) R_(B15) R_(B1) R_(C8)L_(A1516) R_(A44) H H L_(A1517) R_(A44) R_(B1) H L_(A1518) R_(A44)R_(B3) H L_(A1519) R_(A44) R_(B4) H L_(A1520) R_(A44) R_(B5) H L_(A1521)R_(A44) R_(B6) H L_(A1522) R_(A44) R_(B7) H L_(A1523) R_(A44) R_(B24) HL_(A1524) R_(A44) R_(B25) H L_(A1525) R_(A44) R_(A3) H L_(A1526) R_(A44)R_(A34) H L_(A1527) R_(A44) R_(A44) H L_(A1528) R_(A44) R_(A52) HL_(A1529) R_(A44) R_(A53) H L_(A1530) R_(A44) R_(A54) H L_(A1531)R_(A44) R_(C3) H L_(A1532) R_(A44) R_(C4) H L_(A1533) R_(A44) R_(C8) HL_(A1534) R_(A44) H R_(B1) L_(A1535) R_(A44) H R_(B3) L_(A1536) R_(A44)H R_(B4) L_(A1537) R_(A44) H R_(B5) L_(A1538) R_(A44) H R_(B6) L_(A1539)R_(A44) H R_(B7) L_(A1540) R_(A44) H R_(B24) L_(A1541) R_(A44) H R_(B25)L_(A1542) R_(A44) H R_(A3) L_(A1543) R_(A44) H R_(A34) L_(A1544) R_(A44)H R_(A44) L_(A1545) R_(A44) H R_(A52) L_(A1546) R_(A44) H R_(A53)L_(A1547) R_(A44) H R_(A54) L_(A1548) R_(A44) H R_(C3) L_(A1549) R_(A44)H R_(C4) L_(A1550) R_(A44) H R_(C8) L_(A1551) R_(A44) R_(B1) R_(B1)L_(A1552) R_(A44) R_(B3) R_(B1) L_(A1553) R_(A44) R_(B4) R_(B1)L_(A1554) R_(A44) R_(B5) R_(B1) L_(A1555) R_(A44) R_(B6) R_(B1)L_(A1556) R_(A44) R_(B7) R_(B1) L_(A1557) R_(A44) R_(B24) R_(B1)L_(A1558) R_(A44) R_(B25) R_(B1) L_(A1559) R_(A44) R_(A3) R_(B1)L_(A1560) R_(A44) R_(A34) R_(B1) L_(A1561) R_(A44) R_(A44) R_(B1)L_(A1562) R_(A44) R_(A52) R_(B1) L_(A1563) R_(A44) R_(A53) R_(B1)L_(A1564) R_(A44) R_(A54) R_(B1) L_(A1565) R_(A44) R_(C3) R_(B1)L_(A1566) R_(A44) R_(C4) R_(B1) L_(A1567) R_(A44) R_(C8) R_(B1)L_(A1568) R_(A44) R_(B1) R_(B1) L_(A1569) R_(A44) R_(B1) R_(B3)L_(A1570) R_(A44) R_(B1) R_(B4) L_(A1571) R_(A44) R_(B1) R_(B5)L_(A1572) R_(A44) R_(B1) R_(B6) L_(A1573) R_(A44) R_(B1) R_(B7)L_(A1574) R_(A44) R_(B1) R_(B24) L_(A1575) R_(A44) R_(B1) R_(B25)L_(A1576) R_(A44) R_(B1) R_(A3) L_(A1577) R_(A44) R_(B1) R_(A34)L_(A1578) R_(A44) R_(B1) R_(A44) L_(A1579) R_(A44) R_(B1) R_(A52)L_(A1580) R_(A44) R_(B1) R_(A53) L_(A1581) R_(A44) R_(B1) R_(A54)L_(A1582) R_(A44) R_(B1) R_(C3) L_(A1583) R_(A44) R_(B1) R_(C4)L_(A1584) R_(A44) R_(B1) R_(C8)

ligands XLV-L_(Ai-O) that are based on a structure of Formula XLV

where X is O, and ligands XLV-L_(Ai-S) that are based on a structure ofFormula XLV, where X is S; ligands XLVI-L_(Ai-O) that are based on astructure of Formula XLVI

where X is O, and ligands XLVI-L_(Ai-S) that are based on a structure ofFormula XLVI, where X is S; ligands XLVII-L_(Ai-O) that are based on astructure of Formula XLVII

where X is O, and ligands XLVII-L_(Ai-S) that are based on a structureof Formula XLVII, where X is S; ligands XLVIII-L_(Ai-O) that are basedon a structure of Formula XLVIII

where X is O, and ligands XLVIII-L_(Ai-S) that are based on a structureof Formula XLVIII, where X is S; ligands XLIX-L_(Ai-O) that are based ona structure of Formula XLIX

where X is O, and ligands XLIX-L_(Ai-S) that are based on a structure ofFormula XLIX, where X is S, ligands L-L_(Ai-O) that are based on astructure of Formula L

where X is O, and ligands L-L_(Ai-S) that are based on a structure ofFormula L, where X is S; wherein i is an integer from 1654 to 1777 and1847 to 1970 and for each i, R¹, R², R¹¹, and R¹² in the formulas XLVthrough L are defined as follows: L_(Ai) R¹ R⁹ R¹⁰ R² L_(A1654) R_(B1) HH R_(B1) L_(A1655) R_(B1) R_(B1) H R_(B1) L_(A1656) R_(B1) R_(B3) HR_(B1) L_(A1657) R_(B1) R_(B4) H R_(B1) L_(A1658) R_(B1) R_(B5) H R_(B1)L_(A1659) R_(B1) R_(B6) H R_(B1) L_(A1660) R_(B1) R_(B7) H R_(B1)L_(A1661) R_(B1) R_(B24) H R_(B1) L_(A1662) R_(B1) R_(B25) H R_(B1)L_(A1663) R_(B1) R_(A3) H R_(B1) L_(A1664) R_(B1) R_(A34) H R_(B1)L_(A1665) R_(B1) R_(A44) H R_(B1) L_(A1666) R_(B1) R_(A52) H R_(B1)L_(A1667) R_(B1) R_(A53) H R_(B1) L_(A1668) R_(B1) R_(A54) H R_(B1)L_(A1669) R_(B1) R_(C3) H R_(B1) L_(A1670) R_(B1) R_(C4) H R_(B1)L_(A1671) R_(B1) R_(C8) H R_(B1) L_(A1672) R_(B1) H R_(B1) R_(B1)L_(A1673) R_(B1) H R_(B3) R_(B1) L_(A1674) R_(B1) H R_(B4) R_(B1)L_(A1675) R_(B1) H R_(B5) R_(B1) L_(A1676) R_(B1) H R_(B6) R_(B1)L_(A1677) R_(B1) H R_(B7) R_(B1) L_(A1678) R_(B1) H R_(B24) R_(B1)L_(A1679) R_(B1) H R_(B25) R_(B1) L_(A1680) R_(B1) H R_(A3) R_(B1)L_(A1681) R_(B1) H R_(A34) R_(B1) L_(A1682) R_(B1) H R_(A44) R_(B1)L_(A1683) R_(B1) H R_(A52) R_(B1) L_(A1684) R_(B1) H R_(A53) R_(B1)L_(A1685) R_(B1) H R_(A54) R_(B1) L_(A1686) R_(B1) H R_(C3) R_(B1)L_(A1687) R_(B1) H R_(C4) R_(B1) L_(A1688) R_(B1) H R_(C8) R_(B1)L_(A1689) R_(B1) R_(B1) R_(B1) R_(B1) L_(A1690) R_(B1) R_(B3) R_(B1)R_(B1) L_(A1691) R_(B1) R_(B4) R_(B1) R_(B1) L_(A1692) R_(B1) R_(B5)R_(B1) R_(B1) L_(A1693) R_(B1) R_(B6) R_(B1) R_(B1) L_(A1694) R_(B1)R_(B7) R_(B1) R_(B1) L_(A1695) R_(B1) R_(B24) R_(B1) R_(B1) L_(A1696)R_(B1) R_(B25) R_(B1) R_(B1) L_(A1697) R_(B1) R_(A3) R_(B1) R_(B1)L_(A1698) R_(B1) R_(A34) R_(B1) R_(B1) L_(A1699) R_(B1) R_(A44) R_(B1)R_(B1) L_(A1700) R_(B1) R_(A52) R_(B1) R_(B1) L_(A1701) R_(B1) R_(A53)R_(B1) R_(B1) L_(A1702) R_(B1) R_(A54) R_(B1) R_(B1) L_(A1703) R_(B1)R_(C3) R_(B1) R_(B1) L_(A1704) R_(B1) R_(C4) R_(B1) R_(B1) L_(A1705)R_(B1) R_(C8) R_(B1) R_(B1) L_(A1706) R_(B1) R_(B1) R_(B1) R_(B1)L_(A1707) R_(B1) R_(B1) R_(B3) R_(B1) L_(A1708) R_(B1) R_(B1) R_(B4)R_(B1) L_(A1709) R_(B1) R_(B1) R_(B5) R_(B1) L_(A1710) R_(B1) R_(B1)R_(B6) R_(B1) L_(A1711) R_(B1) R_(B1) R_(B7) R_(B1) L_(A1712) R_(B1)R_(B1) R_(B24) R_(B1) L_(A1713) R_(B1) R_(B1) R_(B25) R_(B1) L_(A1714)R_(B1) R_(B1) R_(A3) R_(B1) L_(A1715) R_(B1) R_(B1) R_(A34) R_(B1)L_(A1716) R_(B6) H H R_(B1) L_(A1717) R_(B6) R_(B1) H R_(B1) L_(A1718)R_(B6) R_(B3) H R_(B1) L_(A1719) R_(B6) R_(B4) H R_(B1) L_(A1720) R_(B6)R_(B5) H R_(B1) L_(A1721) R_(B6) R_(B6) H R_(B1) L_(A1722) R_(B6) R_(B7)H R_(B1) L_(A1723) R_(B6) R_(B24) H R_(B1) L_(A1724) R_(B6) R_(B25) HR_(B1) L_(A1725) R_(B6) R_(A3) H R_(B1) L_(A1726) R_(B6) R_(A34) HR_(B1) L_(A1727) R_(B6) R_(A44) H R_(B1) L_(A1728) R_(B6) R_(A52) HR_(B1) L_(A1729) R_(B6) R_(A53) H R_(B1) L_(A1730) R_(B6) R_(A54) HR_(B1) L_(A1731) R_(B6) R_(C3) H R_(B1) L_(A1732) R_(B6) R_(C4) H R_(B1)L_(A1733) R_(B6) R_(C8) H R_(B1) L_(A1734) R_(B6) H R_(B1) R_(B1)L_(A1735) R_(B6) H R_(B3) R_(B1) L_(A1736) R_(B6) H R_(B4) R_(B1)L_(A1737) R_(B6) H R_(B5) R_(B1) L_(A1738) R_(B6) H R_(B6) R_(B1)L_(A1739) R_(B6) H R_(B7) R_(B1) L_(A1740) R_(B6) H R_(B24) R_(B1)L_(A1741) R_(B6) H R_(B25) R_(B1) L_(A1742) R_(B6) H R_(A3) R_(B1)L_(A1743) R_(B6) H R_(A34) R_(B1) L_(A1744) R_(B6) H R_(A44) R_(B1)L_(A1745) R_(B6) H R_(A52) R_(B1) L_(A1746) R_(B6) H R_(A53) R_(B1)L_(A1747) R_(B6) H R_(A54) R_(B1) L_(A1748) R_(B6) H R_(C3) R_(B1)L_(A1749) R_(B6) H R_(C4) R_(B1) L_(A1750) R_(B6) H R_(C8) R_(B1)L_(A1751) R_(B6) R_(B1) R_(B1) R_(B1) L_(A1752) R_(B6) R_(B3) R_(B1)R_(B1) L_(A1753) R_(B6) R_(B4) R_(B1) R_(B1) L_(A1754) R_(B6) R_(B5)R_(B1) R_(B1) L_(A1755) R_(B6) R_(B6) R_(B1) R_(B1) L_(A1756) R_(B6)R_(B7) R_(B1) R_(B1) L_(A1757) R_(B6) R_(B24) R_(B1) R_(B1) L_(A1758)R_(B6) R_(B25) R_(B1) R_(B1) L_(A1759) R_(B6) R_(A3) R_(B1) R_(B1)L_(A1760) R_(B6) R_(A34) R_(B1) R_(B1) L_(A1761) R_(B6) R_(A44) R_(B1)R_(B1) L_(A1762) R_(B6) R_(A52) R_(B1) R_(B1) L_(A1763) R_(B6) R_(A53)R_(B1) R_(B1) L_(A1764) R_(B6) R_(A54) R_(B1) R_(B1) L_(A1765) R_(B6)R_(C3) R_(B1) R_(B1) L_(A1766) R_(B6) R_(C4) R_(B1) R_(B1) L_(A1767)R_(B6) R_(C8) R_(B1) R_(B1) L_(A1768) R_(B6) R_(B1) R_(B1) R_(B1)L_(A1769) R_(B6) R_(B1) R_(B3) R_(B1) L_(A1770) R_(B6) R_(B1) R_(B4)R_(B1) L_(A1771) R_(B6) R_(B1) R_(B5) R_(B1) L_(A1772) R_(B6) R_(B1)R_(B6) R_(B1) L_(A1773) R_(B6) R_(B1) R_(B7) R_(B1) L_(A1774) R_(B6)R_(B1) R_(B24) R_(B1) L_(A1775) R_(B6) R_(B1) R_(B25) R_(B1) L_(A1776)R_(B6) R_(B1) R_(A3) R_(B1) L_(A1777) R_(B6) R_(B1) R_(A34) R_(B1)L_(A1847) R_(B1) H H R_(A54) L_(A1848) R_(B1) R_(B1) H R_(A54) L_(A1849)R_(B1) R_(B3) H R_(A54) L_(A1850) R_(B1) R_(B4) H R_(A54) L_(A1851)R_(B1) R_(B5) H R_(A54) L_(A1852) R_(B1) R_(B6) H R_(A54) L_(A1853)R_(B1) R_(B7) H R_(A54) L_(A1854) R_(B1) R_(B24) H R_(A54) L_(A1855)R_(B1) R_(B25) H R_(A54) L_(A1856) R_(B1) R_(A3) H R_(A54) L_(A1857)R_(B1) R_(A34) H R_(A54) L_(A1858) R_(B1) R_(A44) H R_(A54) L_(A1859)R_(B1) R_(A52) H R_(A54) L_(A1860) R_(B1) R_(A53) H R_(A54) L_(A1861)R_(B1) R_(A54) H R_(A54) L_(A1862) R_(B1) R_(C3) H R_(A54) L_(A1863)R_(B1) R_(C4) H R_(A54) L_(A1864) R_(B1) R_(C8) H R_(A54) L_(A1865)R_(B1) H R_(B1) R_(A54) L_(A1866) R_(B1) H R_(B3) R_(A54) L_(A1867)R_(B1) H R_(B4) R_(A54) L_(A1868) R_(B1) H R_(B5) R_(A54) L_(A1869)R_(B1) H R_(B6) R_(A54) L_(A1870) R_(B1) H R_(B7) R_(A54) L_(A1871)R_(B1) H R_(B24) R_(A54) L_(A1872) R_(B1) H R_(B25) R_(A54) L_(A1873)R_(B1) H R_(A3) R_(A54) L_(A1874) R_(B1) H R_(A34) R_(A54) L_(A1875)R_(B1) H R_(A44) R_(A54) L_(A1876) R_(B1) H R_(A52) R_(A54) L_(A1877)R_(B1) H R_(A53) R_(A54) L_(A1878) R_(B1) H R_(A54) R_(A54) L_(A1879)R_(B1) H R_(C3) R_(A54) L_(A1880) R_(B1) H R_(C4) R_(A54) L_(A1881)R_(B1) H R_(C8) R_(A54) L_(A1882) R_(B1) R_(B1) R_(B1) R_(A54) L_(A1883)R_(B1) R_(B3) R_(B1) R_(A54) L_(A1884) R_(B1) R_(B4) R_(B1) R_(A54)L_(A1885) R_(B1) R_(B5) R_(B1) R_(A54) L_(A1886) R_(B1) R_(B6) R_(B1)R_(A54) L_(A1887) R_(B1) R_(B7) R_(B1) R_(A54) L_(A1888) R_(B1) R_(B24)R_(B1) R_(A54) L_(A1889) R_(B1) R_(B25) R_(B1) R_(A54) L_(A1890) R_(B1)R_(A3) R_(B1) R_(A54) L_(A1891) R_(B1) R_(A34) R_(B1) R_(A54) L_(A1892)R_(B1) R_(A44) R_(B1) R_(A54) L_(A1893) R_(B1) R_(A52) R_(B1) R_(A54)L_(A1894) R_(B1) R_(A53) R_(B1) R_(A54) L_(A1895) R_(B1) R_(A54) R_(B1)R_(A54) L_(A1896) R_(B1) R_(C3) R_(B1) R_(A54) L_(A1897) R_(B1) R_(C4)R_(B1) R_(A54) L_(A1898) R_(B1) R_(C8) R_(B1) R_(A54) L_(A1899) R_(B1)R_(B1) R_(B1) R_(A54) L_(A1900) R_(B1) R_(B1) R_(B3) R_(A54) L_(A1901)R_(B1) R_(B1) R_(B4) R_(A54) L_(A1902) R_(B1) R_(B1) R_(B5) R_(A54)L_(A1903) R_(B1) R_(B1) R_(B6) R_(A54) L_(A1904) R_(B1) R_(B1) R_(B7)R_(A54) L_(A1905) R_(B1) R_(B1) R_(B24) R_(A54) L_(A1906) R_(B1) R_(B1)R_(B25) R_(A54) L_(A1907) R_(B1) R_(B1) R_(A3) R_(A54) L_(A1908) R_(B1)R_(B1) R_(A34) R_(A54) L_(A1909) R_(B6) H H R_(A54) L_(A1910) R_(B6)R_(B1) H R_(A54) L_(A1911) R_(B6) R_(B3) H R_(A54) L_(A1912) R_(B6)R_(B4) H R_(A54) L_(A1913) R_(B6) R_(B5) H R_(A54) L_(A1914) R_(B6)R_(B6) H R_(A54) L_(A1915) R_(B6) R_(B7) H R_(A54) L_(A1916) R_(B6)R_(B24) H R_(A54) L_(A1917) R_(B6) R_(B25) H R_(A54) L_(A1918) R_(B6)R_(A3) H R_(A54) L_(A1919) R_(B6) R_(A34) H R_(A54) L_(A1920) R_(B6)R_(A44) H R_(A54) L_(A1921) R_(B6) R_(A52) H R_(A54) L_(A1922) R_(B6)R_(A53) H R_(A54) L_(A1923) R_(B6) R_(A54) H R_(A54) L_(A1924) R_(B6)R_(C3) H R_(A54) L_(A1925) R_(B6) R_(C4) H R_(A54) L_(A1926) R_(B6)R_(C8) H R_(A54) L_(A1927) R_(B6) H R_(B1) R_(A54) L_(A1928) R_(B6) HR_(B3) R_(A54) L_(A1929) R_(B6) H R_(B4) R_(A54) L_(A1930) R_(B6) HR_(B5) R_(A54) L_(A1931) R_(B6) H R_(B6) R_(A54) L_(A1932) R_(B6) HR_(B7) R_(A54) L_(A1933) R_(B6) H R_(B24) R_(A54) L_(A1934) R_(B6) HR_(B25) R_(A54) L_(A1935) R_(B6) H R_(A3) R_(A54) L_(A1936) R_(B6) HR_(A34) R_(A54) L_(A1937) R_(B6) H R_(A44) R_(A54) L_(A1938) R_(B6) HR_(A52) R_(A54) L_(A1939) R_(B6) H R_(A53) R_(A54) L_(A1940) R_(B6) HR_(A54) R_(A54) L_(A1941) R_(B6) H R_(C3) R_(A54) L_(A1942) R_(B6) HR_(C4) R_(A54) L_(A1943) R_(B6) H R_(C8) R_(A54) L_(A1944) R_(B6) R_(B1)R_(B1) R_(A54) L_(A1945) R_(B6) R_(B3) R_(B1) R_(A54) L_(A1946) R_(B6)R_(B4) R_(B1) R_(A54) L_(A1947) R_(B6) R_(B5) R_(B1) R_(A54) L_(A1948)R_(B6) R_(B6) R_(B1) R_(A54) L_(A1949) R_(B6) R_(B7) R_(B1) R_(A54)L_(A1950) R_(B6) R_(B24) R_(B1) R_(A54) L_(A1951) R_(B6) R_(B25) R_(B1)R_(A54) L_(A1952) R_(B6) R_(A3) R_(B1) R_(A54) L_(A1953) R_(B6) R_(A34)R_(B1) R_(A54) L_(A1954) R_(B6) R_(A44) R_(B1) R_(A54) L_(A1955) R_(B6)R_(A52) R_(B1) R_(A54) L_(A1956) R_(B6) R_(A53) R_(B1) R_(A54) L_(A1957)R_(B6) R_(A54) R_(B1) R_(A54) L_(A1958) R_(B6) R_(C3) R_(B1) R_(A54)L_(A1959) R_(B6) R_(C4) R_(B1) R_(A54) L_(A1960) R_(B6) R_(C8) R_(B1)R_(A54) L_(A1961) R_(B6) R_(B1) R_(B1) R_(A54) L_(A1962) R_(B6) R_(B1)R_(B3) R_(A54) L_(A1963) R_(B6) R_(B1) R_(B4) R_(A54) L_(A1964) R_(B6)R_(B1) R_(B5) R_(A54) L_(A1965) R_(B6) R_(B1) R_(B6) R_(A54) L_(A1966)R_(B6) R_(B1) R_(B7) R_(A54) L_(A1967) R_(B6) R_(B1) R_(B24) R_(A54)L_(A1968) R_(B6) R_(B1) R_(B25) R_(A54) L_(A1969) R_(B6) R_(B1) R_(A3)R_(A54) L_(A1970) R_(B6) R_(B1) R_(A34) R_(A54)

wherein R_(B1) to R_(B25) have the following structures:

wherein R_(A1) to R_(A53) have the following structures:

wherein R_(C1) to R_(C11) have the following structures:


9. The compound of claim 8, wherein the compound is selected from thegroup consisting of structures of formula Ir(L_(A))₂(L_(Bj)), whereinL_(A) is selected from the group consisting of Formula XVIII-L_(A1171-O)to Formula XVIV-L_(A1584-O), Formula XVIII-L_(A1171-S) to FormulaXVIV-L_(A1584-S), Formula XLV-L_(A1654-O) to Formula L-L_(A1777-O),Formula XLV-L_(A1847-O) to Formula L-L_(A1970-O), FormulaXLV-L_(A1654-S) to Formula L-L_(A1777-S), and Formula L-L_(A1847-S) toFormula L-L_(A1970-S), wherein j is an integer from 1 to 1260; andwherein L_(B1) through L_(B17) are defined as follows: L_(B1) throughL_(B1260) are based on a structure,

in which R¹, R², and R³ are defined as: Ligand R¹ R² R³ L_(B1) R^(D1)R^(D1) H L_(B2) R^(D2) R^(D2) H L_(B3) R^(D3) R^(D3) H L_(B4) R^(D4)R^(D4) H L_(B5) R^(D5) R^(D5) H L_(B6) R^(D6) R^(D6) H L_(B7) R^(D7)R^(D7) H L_(B8) R^(D8) R^(D8) H L_(B9) R^(D9) R^(D9) H L_(B10) R^(D10)R^(D10) H L_(B11) R^(D11) R^(D11) H L_(B12) R^(D12) R^(D12) H L_(B13)R^(D13) R^(D13) H L_(B14) R^(D14) R^(D14) H L_(B15) R^(D15) R^(D15) HL_(B16) R^(D16) R^(D16) H L_(B17) R^(D17) R^(D17) H L_(B18) R^(D18)R^(D18) H L_(B19) R^(D19) R^(D19) H L_(B20) R^(D20) R^(D20) H L_(B21)R^(D21) R^(D21) H L_(B22) R^(D22) R^(D22) H L_(B23) R^(D23) R^(D23) HL_(B24) R^(D24) R^(D24) H L_(B25) R^(D25) R^(D25) H L_(B26) R^(D26)R^(D26) H L_(B27) R^(D27) R^(D27) H L_(B28) R^(D28) R^(D28) H L_(B29)R^(D29) R^(D29) H L_(B30) R^(D30) R^(D30) H L_(B31) R^(D31) R^(D31) HL_(B32) R^(D32) R^(D32) H L_(B33) R^(D33) R^(D33) H L_(B34) R^(D34)R^(D34) H L_(B35) R^(D35) R^(D35) H L_(B36) R^(D40) R^(D40) H L_(B37)R^(D41) R^(D41) H L_(B38) R^(D42) R^(D42) H L_(B39) R^(D64) R^(D64) HL_(B40) R^(D66) R^(D66) H L_(B41) R^(D68) R^(D68) H L_(B42) R^(D76)R^(D76) H L_(B43) R^(D1) R^(D2) H L_(B44) R^(D1) R^(D3) H L_(B45) R^(D1)R^(D4) H L_(B46) R^(D1) R^(D5) H L_(B47) R^(D1) R^(D6) H L_(B48) R^(D1)R^(D7) H L_(B49) R^(D1) R^(D8) H L_(B50) R^(D1) R^(D9) H L_(B51) R^(D1)R^(D10) H L_(B52) R^(D1) R^(D11) H L_(B53) R^(D1) R^(D12) H L_(B54)R^(D1) R^(D13) H L_(B55) R^(D1) R^(D14) H L_(B56) R^(D1) R^(D15) HL_(B57) R^(D1) R^(D16) H L_(B58) R^(D1) R^(D17) H L_(B59) R^(D1) R^(D18)H L_(B60) R^(D1) R^(D19) H L_(B61) R^(D1) R^(D20) H L_(B62) R^(D1)R^(D21) H L_(B63) R^(D1) R^(D22) H L_(B64) R^(D1) R^(D23) H L_(B65)R^(D1) R^(D24) H L_(B66) R^(D1) R^(D25) H L_(B67) R^(D1) R^(D26) HL_(B68) R^(D1) R^(D27) H L_(B69) R^(D1) R^(D28) H L_(B70) R^(D1) R^(D29)H L_(B71) R^(D1) R^(D30) H L_(B72) R^(D1) R^(D31) H L_(B73) R^(D1)R^(D32) H L_(B74) R^(D1) R^(D33) H L_(B75) R^(D1) R^(D34) H L_(B76)R^(D1) R^(D35) H L_(B77) R^(D1) R^(D40) H L_(B78) R^(D1) R^(D41) HL_(B79) R^(D1) R^(D42) H L_(B80) R^(D1) R^(D64) H L_(B81) R^(D1) R^(D66)H L_(B82) R^(D1) R^(D68) H L_(B83) R^(D1) R^(D76) H L_(B84) R^(D2)R^(D1) H L_(B85) R^(D2) R^(D3) H L_(B86) R^(D2) R^(D4) H L_(B87) R^(D2)R^(D5) H L_(B88) R^(D2) R^(D6) H L_(B89) R^(D2) R^(D7) H L_(B90) R^(D2)R^(D8) H L_(B91) R^(D2) R^(D9) H L_(B92) R^(D2) R^(D10) H L_(B93) R^(D2)R^(D11) H L_(B94) R^(D2) R^(D12) H L_(B95) R^(D2) R^(D13) H L_(B96)R^(D2) R^(D14) H L_(B97) R^(D2) R^(D15) H L_(B98) R^(D2) R^(D16) HL_(B99) R^(D2) R^(D17) H L_(B100) R^(D2) R^(D18) H L_(B101) R^(D2)R^(D19) H L_(B102) R^(D2) R^(D20) H L_(B103) R^(D2) R^(D21) H L_(B104)R^(D2) R^(D22) H L_(B105) R^(D2) R^(D23) H L_(B106) R^(D2) R^(D24) HL_(B107) R^(D2) R^(D25) H L_(B108) R^(D2) R^(D26) H L_(B109) R^(D2)R^(D27) H L_(B110) R^(D2) R^(D28) H L_(B111) R^(D2) R^(D29) H L_(B112)R^(D2) R^(D30) H L_(B113) R^(D2) R^(D31) H L_(B114) R^(D2) R^(D32) HL_(B115) R^(D2) R^(D33) H L_(B116) R^(D2) R^(D34) H L_(B117) R^(D2)R^(D35) H L_(B118) R^(D2) R^(D40) H L_(B119) R^(D2) R^(D41) H L_(B120)R^(D2) R^(D42) H L_(B121) R^(D2) R^(D64) H L_(B122) R^(D2) R^(D66) HL_(B123) R^(D2) R^(D68) H L_(B124) R^(D2) R^(D76) H L_(B125) R^(D3)R^(D4) H L_(B126) R^(D3) R^(D5) H L_(B127) R^(D3) R^(D6) H L_(B128)R^(D3) R^(D7) H L_(B129) R^(D3) R^(D8) H L_(B130) R^(D3) R^(D9) HL_(B131) R^(D3) R^(D10) H L_(B132) R^(D3) R^(D11) H L_(B133) R^(D3)R^(D12) H L_(B134) R^(D3) R^(D13) H L_(B135) R^(D3) R^(D14) H L_(B136)R^(D3) R^(D15) H L_(B137) R^(D3) R^(D16) H L_(B138) R^(D3) R^(D17) HL_(B139) R^(D3) R^(D18) H L_(B140) R^(D3) R^(D19) H L_(B141) R^(D3)R^(D20) H L_(B142) R^(D3) R^(D21) H L_(B143) R^(D3) R^(D22) H L_(B144)R^(D3) R^(D23) H L_(B145) R^(D3) R^(D24) H L_(B146) R^(D3) R^(D25) HL_(B147) R^(D3) R^(D26) H L_(B148) R^(D3) R^(D27) H L_(B149) R^(D3)R^(D28) H L_(B150) R^(D3) R^(D29) H L_(B151) R^(D3) R^(D30) H L_(B152)R^(D3) R^(D31) H L_(B153) R^(D3) R^(D32) H L_(B154) R^(D3) R^(D33) HL_(B155) R^(D3) R^(D34) H L_(B156) R^(D3) R^(D35) H L_(B157) R^(D3)R^(D40) H L_(B158) R^(D3) R^(D41) H L_(B159) R^(D3) R^(D42) H L_(B160)R^(D3) R^(D64) H L_(B161) R^(D3) R^(D66) H L_(B162) R^(D3) R^(D68) HL_(B163) R^(D3) R^(D76) H L_(B164) R^(D4) R^(D5) H L_(B165) R^(D4)R^(D6) H L_(B166) R^(D4) R^(D7) H L_(B167) R^(D4) R^(D8) H L_(B168)R^(D4) R^(D9) H L_(B169) R^(D4) R^(D10) H L_(B170) R^(D4) R^(D11) HL_(B171) R^(D4) R^(D12) H L_(B172) R^(D4) R^(D13) H L_(B173) R^(D4)R^(D14) H L_(B174) R^(D4) R^(D15) H L_(B175) R^(D4) R^(D16) H L_(B176)R^(D4) R^(D17) H L_(B177) R^(D4) R^(D18) H L_(B178) R^(D4) R^(D19) HL_(B179) R^(D4) R^(D20) H L_(B180) R^(D4) R^(D21) H L_(B181) R^(D4)R^(D22) H L_(B182) R^(D4) R^(D23) H L_(B183) R^(D4) R^(D24) H L_(B184)R^(D4) R^(D25) H L_(B185) R^(D4) R^(D26) H L_(B186) R^(D4) R^(D27) HL_(B187) R^(D4) R^(D28) H L_(B188) R^(D4) R^(D29) H L_(B189) R^(D4)R^(D30) H L_(B190) R^(D4) R^(D31) H L_(B191) R^(D4) R^(D32) H L_(B192)R^(D4) R^(D33) H L_(B193) R^(D4) R^(D34) H L_(B194) R^(D4) R^(D35) HL_(B195) R^(D4) R^(D40) H L_(B196) R^(D4) R^(D41) H L_(B197) R^(D4)R^(D42) H L_(B198) R^(D4) R^(D64) H L_(B199) R^(D4) R^(D66) H L_(B200)R^(D4) R^(D68) H L_(B201) R^(D4) R^(D76) H L_(B202) R^(D4) R^(D1) HL_(B203) R^(D7) R^(D5) H L_(B204) R^(D7) R^(D6) H L_(B205) R^(D7) R^(D8)H L_(B206) R^(D7) R^(D9) H L_(B207) R^(D7) R^(D10) H L_(B208) R^(D7)R^(D11) H L_(B209) R^(D7) R^(D12) H L_(B210) R^(D7) R^(D13) H L_(B211)R^(D7) R^(D14) H L_(B212) R^(D7) R^(D15) H L_(B213) R^(D7) R^(D16) HL_(B214) R^(D7) R^(D17) H L_(B215) R^(D7) R^(D18) H L_(B216) R^(D7)R^(D19) H L_(B217) R^(D7) R^(D20) H L_(B218) R^(D7) R^(D21) H L_(B219)R^(D7) R^(D22) H L_(B220) R^(D7) R^(D23) H L_(B221) R^(D7) R^(D24) HL_(B222) R^(D7) R^(D25) H L_(B223) R^(D7) R^(D26) H L_(B224) R^(D7)R^(D27) H L_(B225) R^(D7) R^(D28) H L_(B226) R^(D7) R^(D29) H L_(B227)R^(D7) R^(D30) H L_(B228) R^(D7) R^(D31) H L_(B229) R^(D7) R^(D32) HL_(B230) R^(D7) R^(D33) H L_(B231) R^(D7) R^(D34) H L_(B232) R^(D7)R^(D35) H L_(B233) R^(D7) R^(D40) H L_(B234) R^(D7) R^(D41) H L_(B235)R^(D7) R^(D42) H L_(B236) R^(D7) R^(D64) H L_(B237) R^(D7) R^(D66) HL_(B238) R^(D7) R^(D68) H L_(B239) R^(D7) R^(D76) H L_(B240) R^(D8)R^(D5) H L_(B241) R^(D8) R^(D6) H L_(B242) R^(D8) R^(D9) H L_(B243)R^(D8) R^(D10) H L_(B244) R^(D8) R^(D11) H L_(B245) R^(D8) R^(D12) HL_(B246) R^(D8) R^(D13) H L_(B247) R^(D8) R^(D14) H L_(B248) R^(D8)R^(D15) H L_(B249) R^(D8) R^(D16) H L_(B250) R^(D8) R^(D17) H L_(B251)R^(D8) R^(D18) H L_(B252) R^(D8) R^(D19) H L_(B253) R^(D8) R^(D20) HL_(B254) R^(D8) R^(D21) H L_(B255) R^(D8) R^(D22) H L_(B256) R^(D8)R^(D23) H L_(B257) R^(D8) R^(D24) H L_(B258) R^(D8) R^(D25) H L_(B259)R^(D8) R^(D26) H L_(B260) R^(D8) R^(D27) H L_(B261) R^(D8) R^(D28) HL_(B262) R^(D8) R^(D29) H L_(B263) R^(D8) R^(D30) H L_(B264) R^(D8)R^(D31) H L_(B265) R^(D8) R^(D32) H L_(B266) R^(D8) R^(D33) H L_(B267)R^(D8) R^(D34) H L_(B268) R^(D8) R^(D35) H L_(B269) R^(D8) R^(D40) HL_(B270) R^(D8) R^(D41) H L_(B271) R^(D8) R^(D42) H L_(B272) R^(D8)R^(D64) H L_(B273) R^(D8) R^(D66) H L_(B274) R^(D8) R^(D68) H L_(B275)R^(D8) R^(D76) H L_(B276) R^(D11) R^(D5) H L_(B277) R^(D11) R^(D6) HL_(B278) R^(D11) R^(D9) H L_(B279) R^(D11) R^(D10) H L_(B280) R^(D11)R^(D12) H L_(B281) R^(D11) R^(D13) H L_(B282) R^(D11) R^(D14) H L_(B283)R^(D11) R^(D15) H L_(B284) R^(D11) R^(D16) H L_(B285) R^(D11) R^(D17) HL_(B286) R^(D11) R^(D18) H L_(B287) R^(D11) R^(D19) H L_(B288) R^(D11)R^(D20) H L_(B289) R^(D11) R^(D21) H L_(B290) R^(D11) R^(D22) H L_(B291)R^(D11) R^(D23) H L_(B292) R^(D11) R^(D24) H L_(B293) R^(D11) R^(D25) HL_(B294) R^(D11) R^(D26) H L_(B295) R^(D11) R^(D27) H L_(B296) R^(D11)R^(D28) H L_(B297) R^(D11) R^(D29) H L_(B298) R^(D11) R^(D30) H L_(B299)R^(D11) R^(D31) H L_(B300) R^(D11) R^(D32) H L_(B301) R^(D11) R^(D33) HL_(B302) R^(D11) R^(D34) H L_(B303) R^(D11) R^(D35) H L_(B304) R^(D11)R^(D40) H L_(B305) R^(D11) R^(D41) H L_(B306) R^(D11) R^(D42) H L_(B307)R^(D11) R^(D64) H L_(B308) R^(D11) R^(D66) H L_(B309) R^(D11) R^(D68) HL_(B310) R^(D11) R^(D76) H L_(B311) R^(D13) R^(D5) H L_(B312) R^(D13)R^(D6) H L_(B313) R^(D13) R^(D9) H L_(B314) R^(D13) R^(D10) H L_(B315)R^(D13) R^(D12) H L_(B316) R^(D13) R^(D14) H L_(B317) R^(D13) R^(D15) HL_(B318) R^(D13) R^(D16) H L_(B319) R^(D13) R^(D17) H L_(B320) R^(D13)R^(D18) H L_(B321) R^(D13) R^(D19) H L_(B322) R^(D13) R^(D0) H L_(B323)R^(D13) R^(D21) H L_(B324) R^(D13) R^(D22) H L_(B325) R^(D13) R^(D23) HL_(B326) R^(D13) R^(D24) H L_(B327) R^(D13) R^(D25) H L_(B328) R^(D13)R^(D26) H L_(B329) R^(D13) R^(D27) H L_(B330) R^(D13) R^(D28) H L_(B331)R^(D13) R^(D29) H L_(B332) R^(D13) R^(D30) H L_(B333) R^(D13) R^(D31) HL_(B334) R^(D13) R^(D32) H L_(B335) R^(D13) R^(D33) H L_(B336) R^(D13)R^(D34) H L_(B337) R^(D13) R^(D35) H L_(B338) R^(D13) R^(D40) H L_(B339)R^(D13) R^(D41) H L_(B340) R^(D13) R^(D42) H L_(B341) R^(D13) R^(D64) HL_(B342) R^(D13) R^(D66) H L_(B343) R^(D13) R^(D68) H L_(B344) R^(D13)R^(D76) H L_(B345) R^(D14) R^(D5) H L_(B346) R^(D14) R^(D6) H L_(B347)R^(D14) R^(D9) H L_(B348) R^(D14) R^(D10) H L_(B349) R^(D14) R^(D12) HL_(B350) R^(D14) R^(D15) H L_(B351) R^(D14) R^(D16) H L_(B352) R^(D14)R^(D17) H L_(B353) R^(D14) R^(D18) H L_(B354) R^(D14) R^(D19) H L_(B355)R^(D14) R^(D20) H L_(B356) R^(D14) R^(D21) H L_(B357) R^(D14) R^(D22) HL_(B358) R^(D14) R^(D23) H L_(B359) R^(D14) R^(D24) H L_(B360) R^(D14)R^(D25) H L_(B361) R^(D14) R^(D26) H L_(B362) R^(D14) R^(D27) H L_(B363)R^(D14) R^(D28) H L_(B364) R^(D14) R^(D29) H L_(B365) R^(D14) R^(D30) HL_(B366) R^(D14) R^(D31) H L_(B367) R^(D14) R^(D32) H L_(B368) R^(D14)R^(D33) H L_(B369) R^(D14) R^(D34) H L_(B370) R^(D14) R^(D35) H L_(B371)R^(D14) R^(D40) H L_(B372) R^(D14) R^(D41) H L_(B373) R^(D14) R^(D42) HL_(B374) R^(D14) R^(D64) H L_(B375) R^(D14) R^(D66) H L_(B376) R^(D14)R^(D68) H L_(B377) R^(D14) R^(D76) H L_(B378) R^(D22) R^(D5) H L_(B379)R^(D22) R^(D6) H L_(B380) R^(D22) R^(D9) H L_(B381) R^(D22) R^(D10) HL_(B382) R^(D22) R^(D12) H L_(B383) R^(D22) R^(D15) H L_(B384) R^(D22)R^(D16) H L_(B385) R^(D22) R^(D17) H L_(B386) R^(D22) R^(D18) H L_(B387)R^(D22) R^(D19) H L_(B388) R^(D22) R^(D20) H L_(B389) R^(D22) R^(D21) HL_(B390) R^(D22) R^(D23) H L_(B391) R^(D22) R^(D24) H L_(B392) R^(D22)R^(D25) H L_(B393) R^(D22) R^(D26) H L_(B394) R^(D22) R^(D27) H L_(B395)R^(D22) R^(D28) H L_(B396) R^(D22) R^(D29) H L_(B397) R^(D22) R^(D30) HL_(B398) R^(D22) R^(D31) H L_(B399) R^(D22) R^(D32) H L_(B400) R^(D22)R^(D33) H L_(B401) R^(D22) R^(D34) H L_(B402) R^(D22) R^(D35) H L_(B403)R^(D22) R^(D40) H L_(B404) R^(D22) R^(D41) H L_(B405) R^(D22) R^(D42) HL_(B406) R^(D22) R^(D64) H L_(B407) R^(D22) R^(D66) H L_(B408) R^(D22)R^(D68) H L_(B409) R^(D22) R^(D76) H L_(B410) R^(D26) R^(D5) H L_(B411)R^(D26) R^(D6) H L_(B412) R^(D26) R^(D9) H L_(B413) R^(D26) R^(D10) HL_(B414) R^(D26) R^(D12) H L_(B415) R^(D26) R^(D15) H L_(B416) R^(D26)R^(D16) H L_(B417) R^(D26) R^(D17) H L_(B418) R^(D26) R^(D18) H L_(B419)R^(D26) R^(D19) H L_(B420) R^(D26) R^(D20) H L_(B421) R^(D26) R^(D21) HL_(B422) R^(D26) R^(D23) H L_(B423) R^(D26) R^(D24) H L_(B424) R^(D26)R^(D25) H L_(B425) R^(D26) R^(D27) H L_(B426) R^(D26) R^(D28) H L_(B427)R^(D26) R^(D29) H L_(B428) R^(D26) R^(D30) H L_(B429) R^(D26) R^(D31) HL_(B430) R^(D26) R^(D32) H L_(B431) R^(D26) R^(D33) H L_(B432) R^(D26)R^(D34) H L_(B433) R^(D26) R^(D35) H L_(B434) R^(D26) R^(D40) H L_(B435)R^(D26) R^(D41) H L_(B436) R^(D26) R^(D42) H L_(B437) R^(D26) R^(D64) HL_(B438) R^(D26) R^(D66) H L_(B439) R^(D26) R^(D68) H L_(B440) R^(D26)R^(D76) H L_(B441) R^(D35) R^(D5) H L_(B442) R^(D35) R^(D6) H L_(B443)R^(D35) R^(D9) H L_(B444) R^(D35) R^(D10) H L_(B445) R^(D35) R^(D12) HL_(B446) R^(D35) R^(D15) H L_(B447) R^(D35) R^(D16) H L_(B448) R^(D35)R^(D17) H L_(B449) R^(D35) R^(D18) H L_(B450) R^(D35) R^(D19) H L_(B451)R^(D35) R^(D20) H L_(B452) R^(D35) R^(D21) H L_(B453) R^(D35) R^(D23) HL_(B454) R^(D35) R^(D24) H L_(B455) R^(D35) R^(D25) H L_(B456) R^(D35)R^(D27) H L_(B457) R^(D35) R^(D28) H L_(B458) R^(D35) R^(D29) H L_(B459)R^(D35) R^(D30) H L_(B460) R^(D35) R^(D31) H L_(B461) R^(D35) R^(D32) HL_(B462) R^(D35) R^(D33) H L_(B463) R^(D35) R^(D34) H L_(B464) R^(D35)R^(D40) H L_(B465) R^(D35) R^(D41) H L_(B466) R^(D35) R^(D42) H L_(B467)R^(D35) R^(D64) H L_(B468) R^(D35) R^(D66) H L_(B469) R^(D35) R^(D68) HL_(B470) R^(D35) R^(D76) H L_(B471) R^(D40) R^(D5) H L_(B472) R^(D40)R^(D6) H L_(B473) R^(D40) R^(D9) H L_(B474) R^(D40) R^(D10) H L_(B475)R^(D40) R^(D12) H L_(B476) R^(D40) R^(D15) H L_(B477) R^(D40) R^(D16) HL_(B478) R^(D40) R^(D17) H L_(B479) R^(D40) R^(D18) H L_(B480) R^(D40)R^(D19) H L_(B481) R^(D40) R^(D20) H L_(B482) R^(D40) R^(D21) H L_(B483)R^(D40) R^(D23) H L_(B484) R^(D40) R^(D24) H L_(B485) R^(D40) R^(D25) HL_(B486) R^(D40) R^(D27) H L_(B487) R^(D40) R^(D28) H L_(B488) R^(D40)R^(D29) H L_(B489) R^(D40) R^(D30) H L_(B490) R^(D40) R^(D31) H L_(B491)R^(D40) R^(D32) H L_(B492) R^(D40) R^(D33) H L_(B493) R^(D40) R^(D34) HL_(B494) R^(D40) R^(D41) H L_(B495) R^(D40) R^(D42) H L_(B496) R^(D40)R^(D64) H L_(B497) R^(D40) R^(D66) H L_(B498) R^(D40) R^(D68) H L_(B499)R^(D40) R^(D76) H L_(B500) R^(D41) R^(D5) H L_(B501) R^(D41) R^(D6) HL_(B502) R^(D41) R^(D9) H L_(B503) R^(D41) R^(D10) H L_(B504) R^(D41)R^(D12) H L_(B505) R^(D41) R^(D15) H L_(B506) R^(D41) R^(D16) H L_(B507)R^(D41) R^(D17) H L_(B508) R^(D41) R^(D18) H L_(B509) R^(D41) R^(D19) HL_(B510) R^(D41) R^(D20) H L_(B511) R^(D41) R^(D21) H L_(B512) R^(D41)R^(D23) H L_(B513) R^(D41) R^(D24) H L_(B514) R^(D41) R^(D25) H L_(B515)R^(D41) R^(D27) H L_(B516) R^(D41) R^(D28) H L_(B517) R^(D41) R^(D29) HL_(B518) R^(D41) R^(D30) H L_(B519) R^(D41) R^(D31) H L_(B520) R^(D41)R^(D32) H L_(B521) R^(D41) R^(D33) H L_(B522) R^(D41) R^(D34) H L_(B523)R^(D41) R^(D42) H L_(B524) R^(D41) R^(D64) H L_(B525) R^(D41) R^(D66) HL_(B526) R^(D41) R^(D68) H L_(B527) R^(D41) R^(D76) H L_(B528) R^(D64)R^(D5) H L_(B529) R^(D64) R^(D6) H L_(B530) R^(D64) R^(D9) H L_(B531)R^(D64) R^(D10) H L_(B532) R^(D64) R^(D12) H L_(B533) R^(D64) R^(D15) HL_(B534) R^(D64) R^(D16) H L_(B535) R^(D64) R^(D17) H L_(B536) R^(D64)R^(D18) H L_(B537) R^(D64) R^(D19) H L_(B538) R^(D64) R^(D20) H L_(B539)R^(D64) R^(D21) H L_(B540) R^(D64) R^(D23) H L_(B541) R^(D64) R^(D24) HL_(B542) R^(D64) R^(D25) H L_(B543) R^(D64) R^(D27) H L_(B544) R^(D64)R^(D28) H L_(B545) R^(D64) R^(D29) H L_(B546) R^(D64) R^(D30) H L_(B547)R^(D64) R^(D31) H L_(B548) R^(D64) R^(D32) H L_(B549) R^(D64) R^(D33) HL_(B550) R^(D64) R^(D34) H L_(B551) R^(D64) R^(D42) H L_(B552) R^(D64)R^(D64) H L_(B553) R^(D64) R^(D66) H L_(B554) R^(D64) R^(D68) H L_(B555)R^(D64) R^(D76) H L_(B556) R^(D66) R^(D5) H L_(B557) R^(D66) R^(D6) HL_(B558) R^(D66) R^(D9) H L_(B559) R^(D66) R^(D10) H L_(B560) R^(D66)R^(D12) H L_(B561) R^(D66) R^(D15) H L_(B562) R^(D66) R^(D16) H L_(B563)R^(D66) R^(D17) H L_(B564) R^(D66) R^(D18) H L_(B565) R^(D66) R^(D19) HL_(B566) R^(D66) R^(D20) H L_(B567) R^(D66) R^(D21) H L_(B568) R^(D66)R^(D23) H L_(B569) R^(D66) R^(D24) H L_(B570) R^(D66) R^(D25) H L_(B571)R^(D66) R^(D27) H L_(B572) R^(D66) R^(D28) H L_(B573) R^(D66) R^(D29) HL_(B574) R^(D66) R^(D30) H L_(B575) R^(D66) R^(D31) H L_(B576) R^(D66)R^(D32) H L_(B577) R^(D66) R^(D33) H L_(B578) R^(D66) R^(D34) H L_(B579)R^(D66) R^(D42) H L_(B580) R^(D66) R^(D68) H L_(B581) R^(D66) R^(D76) HL_(B582) R^(D68) R^(D5) H L_(B583) R^(D68) R^(D6) H L_(B584) R^(D68)R^(D9) H L_(B585) R^(D68) R^(D10) H L_(B586) R^(D68) R^(D12) H L_(B587)R^(D68) R^(D15) H L_(B588) R^(D68) R^(D16) H L_(B589) R^(D68) R^(D17) HL_(B590) R^(D68) R^(D18) H L_(B591) R^(D68) R^(D19) H L_(B592) R^(D68)R^(D20) H L_(B593) R^(D68) R^(D21) H L_(B594) R^(D68) R^(D23) H L_(B595)R^(D68) R^(D24) H L_(B596) R^(D68) R^(D25) H L_(B597) R^(D68) R^(D27) HL_(B598) R^(D68) R^(D28) H L_(B599) R^(D68) R^(D29) H L_(B600) R^(D68)R^(D30) H L_(B601) R^(D68) R^(D31) H L_(B602) R^(D68) R^(D32) H L_(B603)R^(D68) R^(D33) H L_(B604) R^(D68) R^(D34) H L_(B605) R^(D68) R^(D42) HL_(B606) R^(D68) R^(D76) H L_(B607) R^(D76) R^(D5) H L_(B608) R^(D76)R^(D6) H L_(B609) R^(D76) R^(D9) H L_(B610) R^(D76) R^(D10) H L_(B611)R^(D76) R^(D12) H L_(B612) R^(D76) R^(D15) H L_(B613) R^(D76) R^(D16) HL_(B614) R^(D76) R^(D17) H L_(B615) R^(D76) R^(D18) H L_(B616) R^(D76)R^(D19) H L_(B617) R^(D76) R^(D20) H L_(B618) R^(D76) R^(D21) H L_(B619)R^(D76) R^(D23) H L_(B620) R^(D76) R^(D24) H L_(B621) R^(D76) R^(D25) HL_(B622) R^(D76) R^(D27) H L_(B623) R^(D76) R^(D28) H L_(B624) R^(D76)R^(D29) H L_(B625) R^(D76) R^(D30) H L_(B626) R^(D76) R^(D31) H L_(B627)R^(D76) R^(D32) H L_(B628) R^(D76) R^(D33) H L_(B629) R^(D76) R^(D34) HL_(B630) R^(D76) R^(D42) H L_(B631) R^(D1) R^(D1) R^(D1) L_(B632) R^(D2)R^(D2) R^(D1) L_(B633) R^(D3) R^(D3) R^(D1) L_(B634) R^(D4) R^(D4)R^(D1) L_(B635) R^(D5) R^(D5) R^(D1) L_(B636) R^(D6) R^(D6) R^(D1)L_(B637) R^(D7) R^(D7) R^(D1) L_(B638) R^(D8) R^(D8) R^(D1) L_(B639)R^(D9) R^(D9) R^(D1) L_(B640) R^(D10) R^(D10) R^(D1) L_(B641) R^(D11)R^(D11) R^(D1) L_(B642) R^(D12) R^(D12) R^(D1) L_(B643) R^(D13) R^(D13)R^(D1) L_(B644) R^(D14) R^(D14) R^(D1) L_(B645) R^(D15) R^(D15) R^(D1)L_(B646) R^(D16) R^(D16) R^(D1) L_(B647) R^(D17) R^(D17) R^(D1) L_(B648)R^(D18) R^(D18) R^(D1) L_(B649) R^(D19) R^(D19) R^(D1) L_(B650) R^(D20)R^(D20) R^(D1) L_(B651) R^(D21) R^(D21) R^(D1) L_(B652) R^(D22) R^(D22)R^(D1) L_(B653) R^(D23) R^(D23) R^(D1) L_(B654) R^(D24) R^(D24) R^(D1)L_(B655) R^(D25) R^(D25) R^(D1) L_(B656) R^(D26) R^(D26) R^(D1) L_(B657)R^(D27) R^(D27) R^(D1) L_(B658) R^(D28) R^(D28) R^(D1) L_(B659) R^(D29)R^(D29) R^(D1) L_(B660) R^(D30) R^(D30) R^(D1) L_(B661) R^(D31) R^(D31)R^(D1) L_(B662) R^(D32) R^(D32) R^(D1) L_(B663) R^(D33) R^(D33) R^(D1)L_(B664) R^(D34) R^(D34) R^(D1) L_(B665) R^(D35) R^(D35) R^(D1) L_(B666)R^(D40) R^(D40) R^(D1) L_(B667) R^(D41) R^(D41) R^(D1) L_(B668) R^(D42)R^(D42) R^(D1) L_(B669) R^(D64) R^(D64) R^(D1) L_(B670) R^(D66) R^(D66)R^(D1) L_(B671) R^(D68) R^(D68) R^(D1) L_(B672) R^(D76) R^(D76) R^(D1)L_(B673) R^(D1) R^(D2) R^(D1) L_(B674) R^(D1) R^(D3) R^(D1) L_(B675)R^(D1) R^(D4) R^(D1) L_(B676) R^(D1) R^(D5) R^(D1) L_(B677) R^(D1)R^(D6) R^(D1) L_(B678) R^(D1) R^(D7) R^(D1) L_(B679) R^(D1) R^(D8)R^(D1) L_(B680) R^(D1) R^(D9) R^(D1) L_(B681) R^(D1) R^(D10) R^(D1)L_(B682) R^(D1) R^(D11) R^(D1) L_(B683) R^(D1) R^(D12) R^(D1) L_(B684)R^(D1) R^(D13) R^(D1) L_(B685) R^(D1) R^(D14) R^(D1) L_(B686) R^(D1)R^(D15) R^(D1) L_(B687) R^(D1) R^(D16) R^(D1) L_(B688) R^(D1) R^(D17)R^(D1) L_(B689) R^(D1) R^(D18) R^(D1) L_(B690) R^(D1) R^(D19) R^(D1)L_(B691) R^(D1) R^(D20) R^(D1) L_(B692) R^(D1) R^(D21) R^(D1) L_(B693)R^(D1) R^(D22) R^(D1) L_(B694) R^(D1) R^(D23) R^(D1) L_(B695) R^(D1)R^(D24) R^(D1) L_(B696) R^(D1) R^(D25) R^(D1) L_(B697) R^(D1) R^(D26)R^(D1) L_(B698) R^(D1) R^(D27) R^(D1) L_(B699) R^(D1) R^(D28) R^(D1)L_(B700) R^(D1) R^(D29) R^(D1) L_(B701) R^(D1) R^(D30) R^(D1) L_(B702)R^(D1) R^(D31) R^(D1) L_(B703) R^(D1) R^(D32) R^(D1) L_(B704) R^(D1)R^(D33) R^(D1) L_(B705) R^(D1) R^(D34) R^(D1) L_(B706) R^(D1) R^(D35)R^(D1) L_(B707) R^(D1) R^(D40) R^(D1) L_(B708) R^(D1) R^(D41) R^(D1)L_(B709) R^(D1) R^(D42) R^(D1) L_(B710) R^(D1) R^(D64) R^(D1) L_(B711)R^(D1) R^(D66) R^(D1) L_(B712) R^(D1) R^(D68) R^(D1) L_(B713) R^(D1)R^(D76) R^(D1) L_(B714) R^(D2) R^(D1) R^(D1) L_(B715) R^(D2) R^(D3)R^(D1) L_(B716) R^(D2) R^(D4) R^(D1) L_(B717) R^(D2) R^(D5) R^(D1)L_(B718) R^(D2) R^(D6) R^(D1) L_(B719) R^(D2) R^(D7) R^(D1) L_(B720)R^(D2) R^(D8) R^(D1) L_(B721) R^(D2) R^(D9) R^(D1) L_(B722) R^(D2)R^(D10) R^(D1) L_(B723) R^(D2) R^(D11) R^(D1) L_(B724) R^(D2) R^(D12)R^(D1) L_(B725) R^(D2) R^(D13) R^(D1) L_(B726) R^(D2) R^(D14) R^(D1)L_(B727) R^(D2) R^(D15) R^(D1) L_(B728) R^(D2) R^(D16) R^(D1) L_(B729)R^(D2) R^(D17) R^(D1) L_(B730) R^(D2) R^(D18) R^(D1) L_(B731) R^(D2)R^(D19) R^(D1) L_(B732) R^(D2) R^(D20) R^(D1) L_(B733) R^(D2) R^(D21)R^(D1) L_(B734) R^(D2) R^(D22) R^(D1) L_(B735) R^(D2) R^(D23) R^(D1)L_(B736) R^(D2) R^(D24) R^(D1) L_(B737) R^(D2) R^(D25) R^(D1) L_(B738)R^(D2) R^(D26) R^(D1) L_(B739) R^(D2) R^(D27) R^(D1) L_(B740) R^(D2)R^(D28) R^(D1) L_(B741) R^(D2) R^(D29) R^(D1) L_(B742) R^(D2) R^(D30)R^(D1) L_(B743) R^(D2) R^(D31) R^(D1) L_(B744) R^(D2) R^(D32) R^(D1)L_(B745) R^(D2) R^(D33) R^(D1) L_(B746) R^(D2) R^(D34) R^(D1) L_(B747)R^(D2) R^(D35) R^(D1) L_(B748) R^(D2) R^(D40) R^(D1) L_(B749) R^(D2)R^(D41) R^(D1) L_(B750) R^(D2) R^(D42) R^(D1) L_(B751) R^(D2) R^(D64)R^(D1) L_(B752) R^(D2) R^(D66) R^(D1) L_(B753) R^(D2) R^(D68) R^(D1)L_(B754) R^(D2) R^(D76) R^(D1) L_(B755) R^(D3) R^(D4) R^(D1) L_(B756)R^(D3) R^(D5) R^(D1) L_(B757) R^(D3) R^(D6) R^(D1) L_(B758) R^(D3)R^(D7) R^(D1) L_(B759) R^(D3) R^(D8) R^(D1) L_(B760) R^(D3) R^(D9)R^(D1) L_(B761) R^(D3) R^(D10) R^(D1) L_(B762) R^(D3) R^(D11) R^(D1)L_(B763) R^(D3) R^(D12) R^(D1) L_(B764) R^(D3) R^(D13) R^(D1) L_(B765)R^(D3) R^(D14) R^(D1) L_(B766) R^(D3) R^(D15) R^(D1) L_(B767) R^(D3)R^(D16) R^(D1) L_(B768) R^(D3) R^(D17) R^(D1) L_(B769) R^(D3) R^(D18)R^(D1) L_(B770) R^(D3) R^(D19) R^(D1) L_(B771) R^(D3) R^(D20) R^(D1)L_(B772) R^(D3) R^(D21) R^(D1) L_(B773) R^(D3) R^(D22) R^(D1) L_(B774)R^(D3) R^(D23) R^(D1) L_(B775) R^(D3) R^(D24) R^(D1) L_(B776) R^(D3)R^(D25) R^(D1) L_(B777) R^(D3) R^(D26) R^(D1) L_(B778) R^(D3) R^(D27)R^(D1) L_(B779) R^(D3) R^(D28) R^(D1) L_(B780) R^(D3) R^(D29) R^(D1)L_(B781) R^(D3) R^(D30) R^(D1) L_(B782) R^(D3) R^(D31) R^(D1) L_(B783)R^(D3) R^(D32) R^(D1) L_(B784) R^(D3) R^(D33) R^(D1) L_(B785) R^(D3)R^(D34) R^(D1) L_(B786) R^(D3) R^(D35) R^(D1) L_(B787) R^(D3) R^(D40)R^(D1) L_(B788) R^(D3) R^(D41) R^(D1) L_(B789) R^(D3) R^(D42) R^(D1)L_(B790) R^(D3) R^(D64) R^(D1) L_(B791) R^(D3) R^(D66) R^(D1) L_(B792)R^(D3) R^(D68) R^(D1) L_(B793) R^(D3) R^(D76) R^(D1) L_(B794) R^(D4)R^(D5) R^(D1) L_(B795) R^(D4) R^(D6) R^(D1) L_(B796) R^(D4) R^(D7)R^(D1) L_(B797) R^(D4) R^(D8) R^(D1) L_(B798) R^(D4) R^(D9) R^(D1)L_(B799) R^(D4) R^(D10) R^(D1) L_(B800) R^(D4) R^(D11) R^(D1) L_(B801)R^(D4) R^(D12) R^(D1) L_(B802) R^(D4) R^(D13) R^(D1) L_(B803) R^(D4)R^(D14) R^(D1) L_(B804) R^(D4) R^(D15) R^(D1) L_(B805) R^(D4) R^(D16)R^(D1) L_(B806) R^(D4) R^(D17) R^(D1) L_(B807) R^(D4) R^(D18) R^(D1)L_(B808) R^(D4) R^(D19) R^(D1) L_(B809) R^(D4) R^(D20) R^(D1) L_(B810)R^(D4) R^(D21) R^(D1) L_(B811) R^(D4) R^(D22) R^(D1) L_(B812) R^(D4)R^(D23) R^(D1) L_(B813) R^(D4) R^(D24) R^(D1) L_(B814) R^(D4) R^(D25)R^(D1) L_(B815) R^(D4) R^(D26) R^(D1) L_(B816) R^(D4) R^(D27) R^(D1)L_(B817) R^(D4) R^(D28) R^(D1) L_(B818) R^(D4) R^(D29) R^(D1) L_(B819)R^(D4) R^(D30) R^(D1) L_(B820) R^(D4) R^(D31) R^(D1) L_(B821) R^(D4)R^(D32) R^(D1) L_(B822) R^(D4) R^(D33) R^(D1) L_(B823) R^(D4) R^(D34)R^(D1) L_(B824) R^(D4) R^(D35) R^(D1) L_(B825) R^(D4) R^(D40) R^(D1)L_(B826) R^(D4) R^(D41) R^(D1) L_(B827) R^(D4) R^(D42) R^(D1) L_(B828)R^(D4) R^(D64) R^(D1) L_(B829) R^(D4) R^(D66) R^(D1) L_(B830) R^(D4)R^(D68) R^(D1) L_(B831) R^(D4) R^(D76) R^(D1) L_(B832) R^(D4) R^(D1)R^(D1) L_(B833) R^(D7) R^(D5) R^(D1) L_(B834) R^(D7) R^(D6) R^(D1)L_(B835) R^(D7) R^(D8) R^(D1) L_(B836) R^(D7) R^(D9) R^(D1) L_(B837)R^(D7) R^(D10) R^(D1) L_(B838) R^(D7) R^(D11) R^(D1) L_(B839) R^(D7)R^(D12) R^(D1) L_(B840) R^(D7) R^(D13) R^(D1) L_(B841) R^(D7) R^(D14)R^(D1) L_(B842) R^(D7) R^(D15) R^(D1) L_(B843) R^(D7) R^(D16) R^(D1)L_(B844) R^(D7) R^(D17) R^(D1) L_(B845) R^(D7) R^(D18) R^(D1) L_(B846)R^(D7) R^(D19) R^(D1) L_(B847) R^(D7) R^(D20) R^(D1) L_(B848) R^(D7)R^(D21) R^(D1) L_(B849) R^(D7) R^(D22) R^(D1) L_(B850) R^(D7) R^(D23)R^(D1) L_(B851) R^(D7) R^(D24) R^(D1) L_(B852) R^(D7) R^(D25) R^(D1)L_(B853) R^(D7) R^(D26) R^(D1) L_(B854) R^(D7) R^(D27) R^(D1) L_(B855)R^(D7) R^(D28) R^(D1) L_(B856) R^(D7) R^(D29) R^(D1) L_(B857) R^(D7)R^(D30) R^(D1) L_(B858) R^(D7) R^(D31) R^(D1) L_(B859) R^(D7) R^(D32)R^(D1) L_(B860) R^(D7) R^(D33) R^(D1) L_(B861) R^(D7) R^(D34) R^(D1)L_(B862) R^(D7) R^(D35) R^(D1) L_(B863) R^(D7) R^(D40) R^(D1) L_(B864)R^(D7) R^(D41) R^(D1) L_(B865) R^(D7) R^(D42) R^(D1) L_(B866) R^(D7)R^(D64) R^(D1) L_(B867) R^(D7) R^(D66) R^(D1) L_(B868) R^(D7) R^(D68)R^(D1) L_(B869) R^(D7) R^(D76) R^(D1) L_(B870) R^(D8) R^(D5) R^(D1)L_(B871) R^(D8) R^(D6) R^(D1) L_(B872) R^(D8) R^(D9) R^(D1) L_(B873)R^(D8) R^(D10) R^(D1) L_(B874) R^(D8) R^(D11) R^(D1) L_(B875) R^(D8)R^(D12) R^(D1) L_(B876) R^(D8) R^(D13) R^(D1) L_(B877) R^(D8) R^(D14)R^(D1) L_(B878) R^(D8) R^(D15) R^(D1) L_(B879) R^(D8) R^(D16) R^(D1)L_(B880) R^(D8) R^(D17) R^(D1) L_(B881) R^(D8) R^(D18) R^(D1) L_(B882)R^(D8) R^(D19) R^(D1) L_(B883) R^(D8) R^(D20) R^(D1) L_(B884) R^(D8)R^(D21) R^(D1) L_(B885) R^(D8) R^(D22) R^(D1) L_(B886) R^(D8) R^(D23)R^(D1) L_(B887) R^(D8) R^(D24) R^(D1) L_(B888) R^(D8) R^(D25) R^(D1)L_(B889) R^(D8) R^(D26) R^(D1) L_(B890) R^(D8) R^(D27) R^(D1) L_(B891)R^(D8) R^(D28) R^(D1) L_(B892) R^(D8) R^(D29) R^(D1) L_(B893) R^(D8)R^(D30) R^(D1) L_(B894) R^(D8) R^(D31) R^(D1) L_(B895) R^(D8) R^(D32)R^(D1) L_(B896) R^(D8) R^(D33) R^(D1) L_(B897) R^(D8) R^(D34) R^(D1)L_(B898) R^(D8) R^(D35) R^(D1) L_(B899) R^(D8) R^(D40) R^(D1) L_(B900)R^(D8) R^(D41) R^(D1) L_(B901) R^(D8) R^(D42) R^(D1) L_(B902) R^(D8)R^(D64) R^(D1) L_(B903) R^(D8) R^(D66) R^(D1) L_(B904) R^(D8) R^(D68)R^(D1) L_(B905) R^(D8) R^(D76) R^(D1) L_(B906) R^(D11) R^(D5) R^(D1)L_(B907) R^(D11) R^(D6) R^(D1) L_(B908) R^(D11) R^(D9) R^(D1) L_(B909)R^(D11) R^(D10) R^(D1) L_(B910) R^(D11) R^(D12) R^(D1) L_(B911) R^(D11)R^(D13) R^(D1) L_(B912) R^(D11) R^(D14) R^(D1) L_(B913) R^(D11) R^(D15)R^(D1) L_(B914) R^(D11) R^(D16) R^(D1) L_(B915) R^(D11) R^(D17) R^(D1)L_(B916) R^(D11) R^(D18) R^(D1) L_(B917) R^(D11) R^(D19) R^(D1) L_(B918)R^(D11) R^(D20) R^(D1) L_(B919) R^(D11) R^(D21) R^(D1) L_(B920) R^(D11)R^(D22) R^(D1) L_(B921) R^(D11) R^(D23) R^(D1) L_(B922) R^(D11) R^(D24)R^(D1) L_(B923) R^(D11) R^(D25) R^(D1) L_(B924) R^(D11) R^(D26) R^(D1)L_(B925) R^(D11) R^(D27) R^(D1) L_(B926) R^(D11) R^(D28) R^(D1) L_(B927)R^(D11) R^(D29) R^(D1) L_(B928) R^(D11) R^(D30) R^(D1) L_(B929) R^(D11)R^(D31) R^(D1) L_(B930) R^(D11) R^(D32) R^(D1) L_(B931) R^(D11) R^(D33)R^(D1) L_(B932) R^(D11) R^(D34) R^(D1) L_(B933) R^(D11) R^(D35) R^(D1)L_(B934) R^(D11) R^(D40) R^(D1) L_(B935) R^(D11) R^(D41) R^(D1) L_(B936)R^(D11) R^(D42) R^(D1) L_(B937) R^(D11) R^(D64) R^(D1) L_(B938) R^(D11)R^(D66) R^(D1) L_(B939) R^(D11) R^(D68) R^(D1) L_(B940) R^(D11) R^(D76)R^(D1) L_(B941) R^(D13) R^(D5) R^(D1) L_(B942) R^(D13) R^(D6) R^(D1)L_(B943) R^(D13) R^(D9) R^(D1) L_(B944) R^(D13) R^(D10) R^(D1) L_(B945)R^(D13) R^(D12) R^(D1) L_(B946) R^(D13) R^(D14) R^(D1) L_(B947) R^(D13)R^(D15) R^(D1) L_(B948) R^(D13) R^(D16) R^(D1) L_(B949) R^(D13) R^(D17)R^(D1) L_(B950) R^(D13) R^(D18) R^(D1) L_(B951) R^(D13) R^(D19) R^(D1)L_(B952) R^(D13) R^(D20) R^(D1) L_(B953) R^(D13) R^(D21) R^(D1) L_(B954)R^(D13) R^(D22) R^(D1) L_(B955) R^(D13) R^(D23) R^(D1) L_(B956) R^(D13)R^(D24) R^(D1) L_(B957) R^(D13) R^(D25) R^(D1) L_(B958) R^(D13) R^(D26)R^(D1) L_(B959) R^(D13) R^(D27) R^(D1) L_(B960) R^(D13) R^(D28) R^(D1)L_(B961) R^(D13) R^(D29) R^(D1) L_(B962) R^(D13) R^(D30) R^(D1) L_(B963)R^(D13) R^(D31) R^(D1) L_(B964) R^(D13) R^(D32) R^(D1) L_(B965) R^(D13)R^(D33) R^(D1) L_(B966) R^(D13) R^(D34) R^(D1) L_(B967) R^(D13) R^(D35)R^(D1) L_(B968) R^(D13) R^(D40) R^(D1) L_(B969) R^(D13) R^(D41) R^(D1)L_(B970) R^(D13) R^(D42) R^(D1) L_(B971) R^(D13) R^(D64) R^(D1) L_(B972)R^(D13) R^(D66) R^(D1) L_(B973) R^(D13) R^(D68) R^(D1) L_(B974) R^(D13)R^(D76) R^(D1) L_(B975) R^(D14) R^(D5) R^(D1) L_(B976) R^(D14) R^(D6)R^(D1) L_(B977) R^(D14) R^(D9) R^(D1) L_(B978) R^(D14) R^(D10) R^(D1)L_(B979) R^(D14) R^(D12) R^(D1) L_(B980) R^(D14) R^(D15) R^(D1) L_(B981)R^(D14) R^(D16) R^(D1) L_(B982) R^(D14) R^(D17) R^(D1) L_(B983) R^(D14)R^(D18) R^(D1) L_(B984) R^(D14) R^(D19) R^(D1) L_(B985) R^(D14) R^(D20)R^(D1) L_(B986) R^(D14) R^(D21) R^(D1) L_(B987) R^(D14) R^(D22) R^(D1)L_(B988) R^(D14) R^(D23) R^(D1) L_(B989) R^(D14) R^(D24) R^(D1) L_(B990)R^(D14) R^(D25) R^(D1) L_(B991) R^(D14) R^(D26) R^(D1) L_(B992) R^(D14)R^(D27) R^(D1) L_(B993) R^(D14) R^(D28) R^(D1) L_(B994) R^(D14) R^(D29)R^(D1) L_(B995) R^(D14) R^(D30) R^(D1) L_(B996) R^(D14) R^(D31) R^(D1)L_(B997) R^(D14) R^(D32) R^(D1) L_(B998) R^(D14) R^(D33) R^(D1) L_(B999)R^(D14) R^(D34) R^(D1) L_(B1000) R^(D14) R^(D35) R^(D1) L_(B1001)R^(D14) R^(D40) R^(D1) L_(B1002) R^(D14) R^(D41) R^(D1) L_(B1003)R^(D14) R^(D42) R^(D1) L_(B1004) R^(D14) R^(D64) R^(D1) L_(B1005)R^(D14) R^(D66) R^(D1) L_(B1006) R^(D14) R^(D68) R^(D1) L_(B1007)R^(D14) R^(D76) R^(D1) L_(B1008) R^(D22) R^(D5) R^(D1) L_(B1009) R^(D22)R^(D6) R^(D1) L_(B1010) R^(D22) R^(D9) R^(D1) L_(B1011) R^(D22) R^(D10)R^(D1) L_(B1012) R^(D22) R^(D12) R^(D1) L_(B1013) R^(D22) R^(D15) R^(D1)L_(B1014) R^(D22) R^(D16) R^(D1) L_(B1015) R^(D22) R^(D17) R^(D1)L_(B1016) R^(D22) R^(D18) R^(D1) L_(B1017) R^(D22) R^(D19) R^(D1)L_(B1018) R^(D22) R^(D20) R^(D1) L_(B1019) R^(D22) R^(D21) R^(D1)L_(B1020) R^(D22) R^(D23) R^(D1) L_(B1021) R^(D22) R^(D24) R^(D1)L_(B1022) R^(D22) R^(D25) R^(D1) L_(B1023) R^(D22) R^(D26) R^(D1)L_(B1024) R^(D22) R^(D27) R^(D1) L_(B1025) R^(D22) R^(D28) R^(D1)L_(B1026) R^(D22) R^(D29) R^(D1) L_(B1027) R^(D22) R^(D30) R^(D1)L_(B1028) R^(D22) R^(D31) R^(D1) L_(B1029) R^(D22) R^(D32) R^(D1)L_(B1030) R^(D22) R^(D33) R^(D1) L_(B1031) R^(D22) R^(D34) R^(D1)L_(B1032) R^(D22) R^(D35) R^(D1) L_(B1033) R^(D22) R^(D40) R^(D1)L_(B1034) R^(D22) R^(D41) R^(D1) L_(B1035) R^(D22) R^(D42) R^(D1)L_(B1036) R^(D22) R^(D64) R^(D1) L_(B1037) R^(D22) R^(D66) R^(D1)L_(B1038) R^(D22) R^(D68) R^(D1) L_(B1039) R^(D22) R^(D76) R^(D1)L_(B1040) R^(D26) R^(D5) R^(D1) L_(B1041) R^(D26) R^(D6) R^(D1)L_(B1042) R^(D26) R^(D9) R^(D1) L_(B1043) R^(D26) R^(D10) R^(D1)L_(B1044) R^(D26) R^(D12) R^(D1) L_(B1045) R^(D26) R^(D15) R^(D1)L_(B1046) R^(D26) R^(D16) R^(D1) L_(B1047) R^(D26) R^(D17) R^(D1)L_(B1048) R^(D26) R^(D18) R^(D1) L_(B1049) R^(D26) R^(D19) R^(D1)L_(B1050) R^(D26) R^(D20) R^(D1) L_(B1051) R^(D26) R^(D21) R^(D1)L_(B1052) R^(D26) R^(D23) R^(D1) L_(B1053) R^(D26) R^(D24) R^(D1)L_(B1054) R^(D26) R^(D25) R^(D1) L_(B1055) R^(D26) R^(D27) R^(D1)L_(B1056) R^(D26) R^(D28) R^(D1) L_(B1057) R^(D26) R^(D29) R^(D1)L_(B1058) R^(D26) R^(D30) R^(D1) L_(B1059) R^(D26) R^(D31) R^(D1)L_(B1060) R^(D26) R^(D32) R^(D1) L_(B1061) R^(D26) R^(D33) R^(D1)L_(B1062) R^(D26) R^(D34) R^(D1) L_(B1063) R^(D26) R^(D35) R^(D1)L_(B1064) R^(D26) R^(D40) R^(D1) L_(B1065) R^(D26) R^(D41) R^(D1)L_(B1066) R^(D26) R^(D42) R^(D1) L_(B1067) R^(D26) R^(D64) R^(D1)L_(B1068) R^(D26) R^(D66) R^(D1) L_(B1069) R^(D26) R^(D68) R^(D1)L_(B1070) R^(D26) R^(D76) R^(D1) L_(B1071) R^(D35) R^(D5) R^(D1)L_(B1072) R^(D35) R^(D6) R^(D1) L_(B1073) R^(D35) R^(D9) R^(D1)L_(B1074) R^(D35) R^(D10) R^(D1) L_(B1075) R^(D35) R^(D12) R^(D1)L_(B1076) R^(D35) R^(D15) R^(D1) L_(B1077) R^(D35) R^(D16) R^(D1)L_(B1078) R^(D35) R^(D17) R^(D1) L_(B1079) R^(D35) R^(D18) R^(D1)L_(B1080) R^(D35) R^(D19) R^(D1) L_(B1081) R^(D35) R^(D20) R^(D1)L_(B1082) R^(D35) R^(D21) R^(D1) L_(B1083) R^(D35) R^(D23) R^(D1)L_(B1084) R^(D35) R^(D24) R^(D1) L_(B1085) R^(D35) R^(D25) R^(D1)L_(B1086) R^(D35) R^(D27) R^(D1) L_(B1087) R^(D35) R^(D28) R^(D1)L_(B1088) R^(D35) R^(D29) R^(D1) L_(B1089) R^(D35) R^(D30) R^(D1)L_(B1090) R^(D35) R^(D31) R^(D1) L_(B1091) R^(D35) R^(D32) R^(D1)L_(B1092) R^(D35) R^(D33) R^(D1) L_(B1093) R^(D35) R^(D34) R^(D1)L_(B1094) R^(D35) R^(D40) R^(D1) L_(B1095) R^(D35) R^(D41) R^(D1)L_(B1096) R^(D35) R^(D42) R^(D1) L_(B1097) R^(D35) R^(D64) R^(D1)L_(B1098) R^(D35) R^(D66) R^(D1) L_(B1099) R^(D35) R^(D68) R^(D1)L_(B1100) R^(D35) R^(D76) R^(D1) L_(B1101) R^(D40) R^(D5) R^(D1)L_(B1102) R^(D40) R^(D6) R^(D1) L_(B1103) R^(D40) R^(D9) R^(D1)L_(B1104) R^(D40) R^(D10) R^(D1) L_(B1105) R^(D40) R^(D12) R^(D1)L_(B1106) R^(D40) R^(D15) R^(D1) L_(B1107) R^(D40) R^(D16) R^(D1)L_(B1108) R^(D40) R^(D17) R^(D1) L_(B1109) R^(D40) R^(D18) R^(D1)L_(B1110) R^(D40) R^(D19) R^(D1) L_(B1111) R^(D40) R^(D20) R^(D1)L_(B1112) R^(D40) R^(D21) R^(D1) L_(B1113) R^(D40) R^(D23) R^(D1)L_(B1114) R^(D40) R^(D24) R^(D1) L_(B1115) R^(D40) R^(D25) R^(D1)L_(B1116) R^(D40) R^(D27) R^(D1) L_(B1117) R^(D40) R^(D28) R^(D1)L_(B1118) R^(D40) R^(D29) R^(D1) L_(B1119) R^(D40) R^(D30) R^(D1)L_(B1120) R^(D40) R^(D31) R^(D1) L_(B1121) R^(D40) R^(D32) R^(D1)L_(B1122) R^(D40) R^(D33) R^(D1) L_(B1123) R^(D40) R^(D34) R^(D1)L_(B1124) R^(D40) R^(D41) R^(D1) L_(B1125) R^(D40) R^(D42) R^(D1)L_(B1126) R^(D40) R^(D64) R^(D1) L_(B1127) R^(D40) R^(D66) R^(D1)L_(B1128) R^(D40) R^(D68) R^(D1) L_(B1129) R^(D40) R^(D76) R^(D1)L_(B1130) R^(D41) R^(D5) R^(D1) L_(B1131) R^(D41) R^(D6) R^(D1)L_(B1132) R^(D41) R^(D9) R^(D1) L_(B1133) R^(D41) R^(D10) R^(D1)L_(B1134) R^(D41) R^(D12) R^(D1) L_(B1135) R^(D41) R^(D15) R^(D1)L_(B1136) R^(D41) R^(D16) R^(D1) L_(B1137) R^(D41) R^(D17) R^(D1)L_(B1138) R^(D41) R^(D18) R^(D1) L_(B1139) R^(D41) R^(D19) R^(D1)L_(B1140) R^(D41) R^(D20) R^(D1) L_(B1141) R^(D41) R^(D21) R^(D1)L_(B1142) R^(D41) R^(D23) R^(D1) L_(B1143) R^(D41) R^(D24) R^(D1)L_(B1144) R^(D41) R^(D25) R^(D1) L_(B1145) R^(D41) R^(D27) R^(D1)L_(B1146) R^(D41) R^(D28) R^(D1) L_(B1147) R^(D41) R^(D29) R^(D1)L_(B1148) R^(D41) R^(D30) R^(D1) L_(B1149) R^(D41) R^(D31) R^(D1)L_(B1150) R^(D41) R^(D32) R^(D1) L_(B1151) R^(D41) R^(D33) R^(D1)L_(B1152) R^(D41) R^(D34) R^(D1) L_(B1153) R^(D41) R^(D42) R^(D1)L_(B1154) R^(D41) R^(D64) R^(D1) L_(B1155) R^(D41) R^(D66) R^(D1)L_(B1156) R^(D41) R^(D68) R^(D1) L_(B1157) R^(D41) R^(D76) R^(D1)L_(B1158) R^(D64) R^(D5) R^(D1) L_(B1159) R^(D64) R^(D6) R^(D1)L_(B1160) R^(D64) R^(D9) R^(D1) L_(B1161) R^(D64) R^(D10) R^(D1)L_(B1162) R^(D64) R^(D12) R^(D1) L_(B1163) R^(D64) R^(D15) R^(D1)L_(B1164) R^(D64) R^(D16) R^(D1) L_(B1165) R^(D64) R^(D17) R^(D1)L_(B1166) R^(D64) R^(D18) R^(D1) L_(B1167) R^(D64) R^(D19) R^(D1)L_(B1168) R^(D64) R^(D20) R^(D1) L_(B1169) R^(D64) R^(D21) R^(D1)L_(B1170) R^(D64) R^(D23) R^(D1) L_(B1171) R^(D64) R^(D24) R^(D1)L_(B1172) R^(D64) R^(D25) R^(D1) L_(B1173) R^(D64) R^(D27) R^(D1)L_(B1174) R^(D64) R^(D28) R^(D1) L_(B1175) R^(D64) R^(D29) R^(D1)L_(B1176) R^(D64) R^(D30) R^(D1) L_(B1177) R^(D64) R^(D31) R^(D1)L_(B1178) R^(D64) R^(D32) R^(D1) L_(B1179) R^(D64) R^(D33) R^(D1)L_(B1180) R^(D64) R^(D34) R^(D1) L_(B1181) R^(D64) R^(D42) R^(D1)L_(B1182) R^(D64) R^(D64) R^(D1) L_(B1183) R^(D64) R^(D66) R^(D1)L_(B1184) R^(D64) R^(D68) R^(D1) L_(B1185) R^(D64) R^(D76) R^(D1)L_(B1186) R^(D66) R^(D5) R^(D1) L_(B1187) R^(D66) R^(D6) R^(D1)L_(B1188) R^(D66) R^(D9) R^(D1) L_(B1189) R^(D66) R^(D10) R^(D1)L_(B1190) R^(D66) R^(D12) R^(D1) L_(B1191) R^(D66) R^(D15) R^(D1)L_(B1192) R^(D66) R^(D16) R^(D1) L_(B1193) R^(D66) R^(D17) R^(D1)L_(B1194) R^(D66) R^(D18) R^(D1) L_(B1195) R^(D66) R^(D19) R^(D1)L_(B1196) R^(D66) R^(D20) R^(D1) L_(B1197) R^(D66) R^(D21) R^(D1)L_(B1198) R^(D66) R^(D23) R^(D1) L_(B1199) R^(D66) R^(D24) R^(D1)L_(B1200) R^(D66) R^(D25) R^(D1) L_(B1201) R^(D66) R^(D27) R^(D1)L_(B1202) R^(D66) R^(D28) R^(D1) L_(B1203) R^(D66) R^(D29) R^(D1)L_(B1204) R^(D66) R^(D30) R^(D1) L_(B1205) R^(D66) R^(D31) R^(D1)L_(B1206) R^(D66) R^(D32) R^(D1) L_(B1207) R^(D66) R^(D33) R^(D1)L_(B1208) R^(D66) R^(D34) R^(D1) L_(B1209) R^(D66) R^(D42) R^(D1)L_(B1210) R^(D66) R^(D68) R^(D1) L_(B1211) R^(D66) R^(D76) R^(D1)L_(B1212) R^(D68) R^(D5) R^(D1) L_(B1213) R^(D68) R^(D6) R^(D1)L_(B1214) R^(D68) R^(D9) R^(D1) L_(B1215) R^(D68) R^(D10) R^(D1)L_(B1216) R^(D68) R^(D12) R^(D1) L_(B1217) R^(D68) R^(D15) R^(D1)L_(B1218) R^(D68) R^(D16) R^(D1) L_(B1219) R^(D68) R^(D17) R^(D1)L_(B1220) R^(D68) R^(D18) R^(D1) L_(B1221) R^(D68) R^(D19) R^(D1)L_(B1222) R^(D68) R^(D20) R^(D1) L_(B1223) R^(D68) R^(D21) R^(D1)L_(B1224) R^(D68) R^(D23) R^(D1) L_(B1225) R^(D68) R^(D24) R^(D1)L_(B1226) R^(D68) R^(D25) R^(D1) L_(B1227) R^(D68) R^(D27) R^(D1)L_(B1228) R^(D68) R^(D28) R^(D1) L_(B1229) R^(D68) R^(D29) R^(D1)L_(B1230) R^(D68) R^(D30) R^(D1) L_(B1231) R^(D68) R^(D31) R^(D1)L_(B1232) R^(D68) R^(D32) R^(D1) L_(B1233) R^(D68) R^(D33) R^(D1)L_(B1234) R^(D68) R^(D34) R^(D1) L_(B1235) R^(D68) R^(D42) R^(D1)L_(B1236) R^(D68) R^(D76) R^(D1) L_(B1237) R^(D76) R^(D5) R^(D1)L_(B1238) R^(D76) R^(D6) R^(D1) L_(B1239) R^(D76) R^(D9) R^(D1)L_(B1240) R^(D76) R^(D10) R^(D1) L_(B1241) R^(D76) R^(D12) R^(D1)L_(B1242) R^(D76) R^(D15) R^(D1) L_(B1243) R^(D76) R^(D16) R^(D1)L_(B1244) R^(D76) R^(D17) R^(D1) L_(B1245) R^(D76) R^(D18) R^(D1)L_(B1246) R^(D76) R^(D19) R^(D1) L_(B1247) R^(D76) R^(D20) R^(D1)L_(B1248) R^(D76) R^(D21) R^(D1) L_(B1249) R^(D76) R^(D23) R^(D1)L_(B1250) R^(D76) R^(D24) R^(D1) L_(B1251) R^(D76) R^(D25) R^(D1)L_(B1252) R^(D76) R^(D27) R^(D1) L_(B1253) R^(D76) R^(D28) R^(D1)L_(B1254) R^(D76) R^(D29) R^(D1) L_(B1255) R^(D76) R^(D30) R^(D1)L_(B1256) R^(D76) R^(D31) R^(D1) L_(B1257) R^(D76) R^(D32) R^(D1)L_(B1258) R^(D76) R^(D33) R^(D1) L_(B1259) R^(D76) R^(D34) R^(D1)L_(B1260) R^(D76) R^(D42) R^(D1)

wherein R^(D1) to R^(D81) has the following structures:


10. The compound of claim 1, wherein the compound has formulaIr(L_(A))₃, Ir(L_(A))(L_(B))₂, Ir(L_(A))₂(L_(B)), Ir(L_(A))₂(L_(C)), orIr(L_(A))(L_(B))(L_(C)); and wherein each L_(A), L_(B), and L_(C) is abidentate ligand, and different from each other.
 11. The compound ofclaim 10, wherein L_(B) is L_(Bj) selected from the group consisting of:L_(B1) through L_(B1260) are based on a structure of Formula

in which R¹, R², and R³ are defined as: L_(Bj) R¹ R² R³ L_(B1) R^(D1)R^(D1) H L_(B2) R^(D2) R^(D2) H L_(B3) R^(D3) R^(D3) H L_(B4) R^(D4)R^(D4) H L_(B5) R^(D5) R^(D5) H L_(B6) R^(D6) R^(D6) H L_(B7) R^(D7)R^(D7) H L_(B8) R^(D8) R^(D8) H L_(B9) R^(D9) R^(D9) H L_(B10) R^(D10)R^(D10) H L_(B11) R^(D11) R^(D11) H L_(B12) R^(D12) R^(D12) H L_(B13)R^(D13) R^(D13) H L_(B14) R^(D14) R^(D14) H L_(B15) R^(D15) R^(D15) HL_(B16) R^(D16) R^(D16) H L_(B17) R^(D17) R^(D17) H L_(B18) R^(D18)R^(D18) H L_(B19) R^(D19) R^(D19) H L_(B20) R^(D20) R^(D20) H L_(B21)R^(D21) R^(D21) H L_(B22) R^(D22) R^(D22) H L_(B23) R^(D23) R^(D23) HL_(B24) R^(D24) R^(D24) H L_(B25) R^(D25) R^(D25) H L_(B26) R^(D26)R^(D26) H L_(B27) R^(D27) R^(D27) H L_(B28) R^(D28) R^(D28) H L_(B29)R²⁹ R^(D29) H L_(B30) R^(D30) R^(D30) H L_(B31) R^(D31) R^(D31) HL_(B32) R^(D32) R^(D32) H L_(B33) R^(D33) R^(D33) H L_(B34) R^(D34)R^(D34) H L_(B35) R^(D35) R^(D35) H L_(B36) R^(D40) R^(D40) H L_(B37)R^(D41) R^(D41) H L_(B38) R^(D42) R^(D42) H L_(B39) R^(D64) R^(D64) HL_(B40) R^(D66) R^(D66) H L_(B41) R^(D68) R^(D68) H L_(B42) R^(D76)R^(D76) H L_(B43) R^(D1) R^(D2) H L_(B44) R^(D1) R^(D3) H L_(B45) R^(D1)R^(D4) H L_(B46) R^(D1) R^(D5) H L_(B47) R^(D1) R^(D6) H L_(B48) R^(D1)R^(D7) H L_(B49) R^(D1) R^(D8) H L_(B50) R^(D1) R^(D9) H L_(B51) R^(D1)R^(D10) H L_(B52) R^(D1) R^(D11) H L_(B53) R^(D1) R^(D12) H L_(B54)R^(D1) R^(D13) H L_(B55) R^(D1) R^(D14) H L_(B56) R^(D1) R^(D15) HL_(B57) R^(D1) R^(D16) H L_(B58) R^(D1) R^(D17) H L_(B59) R^(D1) R^(D18)H L_(B60) R^(D1) R^(D19) H L_(B61) R^(D1) R^(D20) H L_(B62) R^(D1)R^(D21) H L_(B63) R^(D1) R^(D22) H L_(B64) R^(D1) R^(D23) H L_(B65)R^(D1) R^(D24) H L_(B66) R^(D1) R^(D25) H L_(B67) R^(D1) R^(D26) HL_(B68) R^(D1) R^(D27) H L_(B69) R^(D1) R^(D28) H L_(B70) R^(D1) R^(D29)H L_(B71) R^(D1) R^(D30) H L_(B72) R^(D1) R^(D31) H L_(B73) R^(D1)R^(D32) H L_(B74) R^(D1) R^(D33) H L_(B75) R^(D1) R^(D34) H L_(B76)R^(D1) R^(D35) H L_(B77) R^(D1) R^(D40) H L_(B78) R^(D1) R^(D41) HL_(B79) R^(D1) R^(D42) H L_(B80) R^(D1) R^(D64) H L_(B81) R^(D1) R^(D66)H L_(B82) R^(D1) R^(D68) H L_(B83) R^(D1) R^(D76) H L_(B84) R^(D2)R^(D1) H L_(B85) R^(D2) R^(D3) H L_(B86) R^(D2) R^(D4) H L_(B87) R^(D2)R^(D5) H L_(B88) R^(D2) R^(D6) H L_(B89) R^(D2) R^(D7) H L_(B90) R^(D2)R^(D8) H L_(B91) R^(D2) R^(D9) H L_(B92) R^(D2) R^(D10) H L_(B93) R^(D2)R^(D11) H L_(B94) R^(D2) R^(D12) H L_(B95) R^(D2) R^(D13) H L_(B96)R^(D2) R^(D14) H L_(B97) R^(D2) R^(D15) H L_(B98) R^(D2) R^(D16) HL_(B99) R^(D2) R^(D17) H L_(B100) R^(D2) R^(D18) H L_(B101) R^(D2)R^(D19) H L_(B102) R^(D2) R^(D20) H L_(B103) R^(D2) R^(D21) H L_(B104)R^(D2) R^(D22) H L_(B105) R^(D2) R^(D23) H L_(B106) R^(D2) R^(D24) HL_(B107) R^(D2) R^(D25) H L_(B108) R^(D2) R^(D26) H L_(B109) R^(D2)R^(D27) H L_(B110) R^(D2) R^(D28) H L_(B111) R^(D2) R^(D29) H L_(B112)R^(D2) R^(D30) H L_(B113) R^(D2) R^(D31) H L_(B114) R^(D2) R^(D32) HL_(B115) R^(D2) R^(D33) H L_(B116) R^(D2) R^(D34) H L_(B117) R^(D2)R^(D35) H L_(B118) R^(D2) R^(D40) H L_(B119) R^(D2) R^(D41) H L_(B120)R^(D2) R^(D42) H L_(B121) R^(D2) R^(D64) H L_(B122) R^(D2) R^(D66) HL_(B123) R^(D2) R^(D68) H L_(B124) R^(D2) R^(D76) H L_(B125) R^(D3)R^(D4) H L_(B126) R^(D3) R^(D5) H L_(B127) R^(D3) R^(D6) H L_(B128)R^(D3) R^(D7) H L_(B129) R^(D3) R^(D8) H L_(B130) R^(D3) R^(D9) HL_(B131) R^(D3) R^(D10) H L_(B132) R^(D3) R^(D11) H L_(B133) R^(D3)R^(D12) H L_(B134) R^(D3) R^(D13) H L_(B135) R^(D3) R^(D14) H L_(B136)R^(D3) R^(D15) H L_(B137) R^(D3) R^(D16) H L_(B138) R^(D3) R^(D17) HL_(B139) R^(D3) R^(D18) H L_(B140) R^(D3) R^(D19) H L_(B141) R^(D3)R^(D20) H L_(B142) R^(D3) R^(D21) H L_(B143) R^(D3) R^(D22) H L_(B144)R^(D3) R^(D23) H L_(B145) R^(D3) R^(D24) H L_(B146) R^(D3) R^(D25) HL_(B147) R^(D3) R^(D26) H L_(B148) R^(D3) R^(D27) H L_(B149) R^(D3)R^(D28) H L_(B150) R^(D3) R^(D29) H L_(B151) R^(D3) R^(D30) H L_(B152)R^(D3) R^(D31) H L_(B153) R^(D3) R^(D32) H L_(B154) R^(D3) R^(D33) HL_(B155) R^(D3) R^(D34) H L_(B156) R^(D3) R^(D35) H L_(B157) R^(D3)R^(D40) H L_(B158) R^(D3) R^(D41) H L_(B159) R^(D3) R^(D42) H L_(B160)R^(D3) R^(D64) H L_(B161) R^(D3) R^(D66) H L_(B162) R^(D3) R^(D68) HL_(B163) R^(D3) R^(D76) H L_(B164) R^(D4) R^(D5) H L_(B165) R^(D4)R^(D6) H L_(B166) R^(D4) R^(D7) H L_(B167) R^(D4) R^(D8) H L_(B168)R^(D4) R^(D9) H L_(B169) R^(D4) R^(D10) H L_(B170) R^(D4) R^(D11) HL_(B171) R^(D4) R^(D12) H L_(B172) R^(D4) R^(D13) H L_(B173) R^(D4)R^(D14) H L_(B174) R^(D4) R^(D15) H L_(B175) R^(D4) R^(D16) H L_(B176)R^(D4) R^(D17) H L_(B177) R^(D4) R^(D18) H L_(B178) R^(D4) R^(D19) HL_(B179) R^(D4) R^(D20) H L_(B180) R^(D4) R^(D21) H L_(B181) R^(D4)R^(D22) H L_(B182) R^(D4) R^(D23) H L_(B183) R^(D4) R^(D24) H L_(B184)R^(D4) R^(D25) H L_(B185) R^(D4) R^(D26) H L_(B186) R^(D4) R^(D27) HL_(B187) R^(D4) R^(D28) H L_(B188) R^(D4) R^(D29) H L_(B189) R^(D4)R^(D30) H L_(B190) R^(D4) R^(D31) H L_(B191) R^(D4) R^(D32) H L_(B192)R^(D4) R^(D33) H L_(B193) R^(D4) R^(D34) H L_(B194) R^(D4) R^(D35) HL_(B195) R^(D4) R^(D40) H L_(B196) R^(D4) R^(D41) H L_(B197) R^(D4)R^(D42) H L_(B198) R^(D4) R^(D64) H L_(B199) R^(D4) R^(D66) H L_(B200)R^(D4) R^(D68) H L_(B201) R^(D4) R^(D76) H L_(B202) R^(D4) R^(D1) HL_(B203) R^(D7) R^(D5) H L_(B204) R^(D7) R^(D6) H L_(B205) R^(D7) R^(D8)H L_(B206) R^(D7) R^(D9) H L_(B207) R^(D7) R^(D10) H L_(B208) R^(D7)R^(D11) H L_(B209) R^(D7) R^(D12) H L_(B210) R^(D7) R^(D13) H L_(B211)R^(D7) R^(D14) H L_(B212) R^(D7) R^(D15) H L_(B213) R^(D7) R^(D16) HL_(B214) R^(D7) R^(D17) H L_(B215) R^(D7) R^(D18) H L_(B216) R^(D7)R^(D19) H L_(B217) R^(D7) R^(D20) H L_(B218) R^(D7) R^(D21) H L_(B219)R^(D7) R^(D22) H L_(B220) R^(D7) R^(D23) H L_(B221) R^(D7) R^(D24) HL_(B222) R^(D7) R^(D25) H L_(B223) R^(D7) R^(D26) H L_(B224) R^(D7)R^(D27) H L_(B225) R^(D7) R^(D28) H L_(B226) R^(D7) R^(D29) H L_(B227)R^(D7) R^(D30) H L_(B228) R^(D7) R^(D31) H L_(B229) R^(D7) R^(D32) HL_(B230) R^(D7) R^(D33) H L_(B231) R^(D7) R^(D34) H L_(B232) R^(D7)R^(D35) H L_(B233) R^(D7) R^(D40) H L_(B234) R^(D7) R^(D41) H L_(B235)R^(D7) R^(D42) H L_(B236) R^(D7) R^(D64) H L_(B237) R^(D7) R^(D66) HL_(B238) R^(D7) R^(D68) H L_(B239) R^(D7) R^(D76) H L_(B240) R^(D8)R^(D5) H L_(B241) R^(D8) R^(D6) H L_(B242) R^(D8) R^(D9) H L_(B243)R^(D8) R^(D10) H L_(B244) R^(D8) R^(D11) H L_(B245) R^(D8) R^(D12) HL_(B246) R^(D8) R^(D13) H L_(B247) R^(D8) R^(D14) H L_(B248) R^(D8)R^(D15) H L_(B249) R^(D8) R^(D16) H L_(B250) R^(D8) R^(D17) H L_(B251)R^(D8) R^(D18) H L_(B252) R^(D8) R^(D19) H L_(B253) R^(D8) R^(D20) HL_(B254) R^(D8) R^(D21) H L_(B255) R^(D8) R^(D22) H L_(B256) R^(D8)R^(D23) H L_(B257) R^(D8) R^(D24) H L_(B258) R^(D8) R^(D25) H L_(B259)R^(D8) R^(D26) H L_(B260) R^(D8) R^(D27) H L_(B261) R^(D8) R^(D28) HL_(B262) R^(D8) R^(D29) H L_(B263) R^(D8) R^(D30) H L_(B264) R^(D8)R^(D31) H L_(B265) R^(D8) R^(D32) H L_(B266) R^(D8) R^(D33) H L_(B267)R^(D8) R^(D34) H L_(B268) R^(D8) R^(D35) H L_(B269) R^(D8) R^(D40) HL_(B270) R^(D8) R^(D41) H L_(B271) R^(D8) R^(D42) H L_(B272) R^(D8)R^(D64) H L_(B273) R^(D8) R^(D66) H L_(B274) R^(D8) R^(D68) H L_(B275)R^(D8) R^(D76) H L_(B276) R^(D11) R^(D5) H L_(B277) R^(D11) R^(D6) HL_(B278) R^(D11) R^(D9) H L_(B279) R^(D11) R^(D10) H L_(B280) R^(D11)R^(D12) H L_(B281) R^(D11) R^(D13) H L_(B282) R^(D11) R^(D14) H L_(B283)R^(D11) R^(D15) H L_(B284) R^(D11) R^(D16) H L_(B285) R^(D11) R^(D17) HL_(B286) R^(D11) R^(D18) H L_(B287) R^(D11) R^(D19) H L_(B288) R^(D11)R^(D20) H L_(B289) R^(D11) R^(D21) H L_(B290) R^(D11) R^(D22) H L_(B291)R^(D11) R^(D23) H L_(B292) R^(D11) R^(D24) H L_(B293) R^(D11) R^(D25) HL_(B294) R^(D11) R^(D26) H L_(B295) R^(D11) R^(D27) H L_(B296) R^(D11)R^(D28) H L_(B297) R^(D11) R^(D29) H L_(B298) R^(D11) R^(D30) H L_(B299)R^(D11) R^(D31) H L_(B300) R^(D11) R^(D32) H L_(B301) R^(D11) R^(D33) HL_(B302) R^(D11) R^(D34) H L_(B303) R^(D11) R^(D35) H L_(B304) R^(D11)R^(D40) H L_(B305) R^(D11) R^(D41) H L_(B306) R^(D11) R^(D42) H L_(B307)R^(D11) R^(D64) H L_(B308) R^(D11) R^(D66) H L_(B309) R^(D11) R^(D68) HL_(B310) R^(D11) R^(D76) H L_(B311) R^(D13) R^(D5) H L_(B312) R^(D13)R^(D6) H L_(B313) R^(D13) R^(D9) H L_(B314) R^(D13) R^(D10) H L_(B315)R^(D13) R^(D12) H L_(B316) R^(D13) R^(D14) H L_(B317) R^(D13) R^(D15) HL_(B318) R^(D13) R^(D16) H L_(B319) R^(D13) R^(D17) H L_(B320) R^(D13)R^(D18) H L_(B321) R^(D13) R^(D19) H L_(B322) R^(D13) R^(D20) H L_(B323)R^(D13) R^(D21) H L_(B324) R^(D13) R^(D22) H L_(B325) R^(D13) R^(D23) HL_(B326) R^(D13) R^(D24) H L_(B327) R^(D13) R^(D25) H L_(B328) R^(D13)R^(D26) H L_(B329) R^(D13) R^(D27) H L_(B330) R^(D13) R^(D28) H L_(B331)R^(D13) R^(D29) H L_(B332) R^(D13) R^(D30) H L_(B333) R^(D13) R^(D31) HL_(B334) R^(D13) R^(D32) H L_(B335) R^(D13) R^(D33) H L_(B336) R^(D13)R^(D34) H L_(B337) R^(D13) R^(D35) H L_(B338) R^(D13) R^(D40) H L_(B339)R^(D13) R^(D41) H L_(B340) R^(D13) R^(D42) H L_(B341) R^(D13) R^(D64) HL_(B342) R^(D13) R^(D66) H L_(B343) R^(D13) R^(D68) H L_(B344) R^(D13)R^(D76) H L_(B345) R^(D14) R^(D5) H L_(B346) R^(D14) R^(D6) H L_(B347)R^(D14) R^(D9) H L_(B348) R^(D14) R^(D10) H L_(B349) R^(D14) R^(D12) HL_(B350) R^(D14) R^(D15) H L_(B351) R^(D14) R^(D16) H L_(B352) R^(D14)R^(D17) H L_(B353) R^(D14) R^(D18) H L_(B354) R^(D14) R^(D19) H L_(B355)R^(D14) R^(D20) H L_(B356) R^(D14) R^(D21) H L_(B357) R^(D14) R^(D22) HL_(B358) R^(D14) R^(D23) H L_(B359) R^(D14) R^(D24) H L_(B360) R^(D14)R^(D25) H L_(B361) R^(D14) R^(D26) H L_(B362) R^(D14) R^(D27) H L_(B363)R^(D14) R^(D28) H L_(B364) R^(D14) R^(D29) H L_(B365) R^(D14) R^(D30) HL_(B366) R^(D14) R^(D31) H L_(B367) R^(D14) R^(D32) H L_(B368) R^(D14)R^(D33) H L_(B369) R^(D14) R^(D34) H L_(B370) R^(D14) R^(D35) H L_(B371)R^(D14) R^(D40) H L_(B372) R^(D14) R^(D41) H L_(B373) R^(D14) R^(D42) HL_(B374) R^(D14) R^(D64) H L_(B375) R^(D14) R^(D66) H L_(B376) R^(D14)R^(D68) H L_(B377) R^(D14) R^(D76) H L_(B378) R^(D22) R^(D5) H L_(B379)R^(D22) R^(D6) H L_(B380) R^(D22) R^(D9) H L_(B381) R^(D22) R^(D10) HL_(B382) R^(D22) R^(D12) H L_(B383) R^(D22) R^(D15) H L_(B384) R^(D22)R^(D16) H L_(B385) R^(D22) R^(D17) H L_(B386) R^(D22) R^(D18) H L_(B387)R^(D22) R^(D19) H L_(B388) R^(D22) R^(D20) H L_(B389) R^(D22) R^(D21) HL_(B390) R^(D22) R^(D23) H L_(B391) R^(D22) R^(D24) H L_(B392) R^(D22)R^(D25) H L_(B393) R^(D22) R^(D26) H L_(B394) R^(D22) R^(D27) H L_(B395)R^(D22) R^(D28) H L_(B396) R^(D22) R^(D29) H L_(B397) R^(D22) R^(D30) HL_(B398) R^(D22) R^(D31) H L_(B399) R^(D22) R^(D32) H L_(B400) R^(D22)R^(D33) H L_(B401) R^(D22) R^(D34) H L_(B402) R^(D22) R^(D35) H L_(B403)R^(D22) R^(D40) H L_(B404) R^(D22) R^(D41) H L_(B405) R^(D22) R^(D42) HL_(B406) R^(D22) R^(D64) H L_(B407) R^(D22) R^(D66) H L_(B408) R^(D22)R^(D68) H L_(B409) R^(D22) R^(D76) H L_(B410) R^(D26) R^(D5) H L_(B411)R^(D26) R^(D6) H L_(B412) R^(D26) R^(D9) H L_(B413) R^(D26) R^(D10) HL_(B414) R^(D26) R^(D12) H L_(B415) R^(D26) R^(D15) H L_(B416) R^(D26)R^(D16) H L_(B417) R^(D26) R^(D17) H L_(B418) R^(D26) R^(D18) H L_(B419)R^(D26) R^(D19) H L_(B420) R^(D26) R^(D20) H L_(B421) R^(D26) R^(D21) HL_(B422) R^(D26) R^(D23) H L_(B423) R^(D26) R^(D24) H L_(B424) R^(D26)R^(D25) H L_(B425) R^(D26) R^(D27) H L_(B426) R^(D26) R^(D28) H L_(B427)R^(D26) R^(D29) H L_(B428) R^(D26) R^(D30) H L_(B429) R^(D26) R^(D31) HL_(B430) R^(D26) R^(D32) H L_(B431) R^(D26) R^(D33) H L_(B432) R^(D26)R^(D34) H L_(B433) R^(D26) R^(D35) H L_(B434) R^(D26) R^(D40) H L_(B435)R^(D26) R^(D41) H L_(B436) R^(D26) R^(D42) H L_(B437) R^(D26) R^(D64) HL_(B438) R^(D26) R^(D66) H L_(B439) R^(D26) R^(D68) H L_(B440) R^(D26)R^(D76) H L_(B441) R^(D35) R^(D5) H L_(B442) R^(D35) R^(D6) H L_(B443)R^(D35) R^(D9) H L_(B444) R^(D35) R^(D10) H L_(B445) R^(D35) R^(D12) HL_(B446) R^(D35) R^(D15) H L_(B447) R^(D35) R^(D16) H L_(B448) R^(D35)R^(D17) H L_(B449) R^(D35) R^(D18) H L_(B450) R^(D35) R^(R19) H L_(B451)R^(D35) R^(D20) H L_(B432) R^(D35) R^(D21) H L_(B433) R^(D35) R^(D23) HL_(B434) R^(D35) R^(D24) H L_(B433) R^(D35) R^(D25) H L_(B456) R^(D35)R^(D27) H L_(B457) R^(D35) R^(D28) H L_(B458) R^(D35) R^(D29) H L_(B459)R^(D35) R^(D30) H L_(B460) R^(D35) R^(D31) H L_(B461) R^(D35) R^(D32) HL_(B462) R^(D35) R^(D33) H L_(B463) R^(D35) R^(D34) H L_(B464) R^(D35)R^(D40) H L_(B465) R^(D35) R^(D41) H L_(B466) R^(D35) R^(D42) H L_(B467)R^(D35) R^(D64) H L_(B468) R^(D35) R^(D66) H L_(B469) R^(D35) R^(D68) HL_(B470) R^(D35) R^(D76) H L_(B471) R^(D40) R^(D5) H L_(B472) R^(D40)R^(D6) H L_(B473) R^(D40) R^(D9) H L_(B474) R^(D40) R^(D10) H L_(B475)R^(D40) R^(D12) H L_(B476) R^(D40) R^(D15) H L_(B477) R^(D40) R^(D16) HL_(B478) R^(D40) R^(D17) H L_(B479) R^(D40) R^(D18) H L_(B480) R^(D40)R^(D19) H L_(B481) R^(D40) R^(D20) H L_(B482) R^(D40) R^(D21) H L_(B485)R^(D40) R^(D23) H L_(B484) R^(D40) R^(D24) H L_(B485) R^(D40) R^(D25) HL_(B486) R^(D40) R^(D27) H L_(B487) R^(D40) R^(D28) H L_(B488) R^(D40)R^(D29) H L_(B489) R^(D40) R^(D30) H L_(B490) R^(D40) R^(D31) H L_(B491)R^(D40) R^(D32) H L_(B492) R^(D40) R^(D33) H L_(B493) R^(D40) R^(D34) HL_(B494) R^(D40) R^(D41) H L_(B495) R^(D40) R^(D42) H L_(B496) R^(D40)R^(D64) H L_(B497) R^(D40) R^(D66) H L_(B498) R^(D40) R^(D68) H L_(B499)R^(D40) R^(D76) H L_(B500) R^(D41) R^(D5) H L_(B501) R^(D41) R^(D6) HL_(B502) R^(D41) R^(D9) H L_(B503) R^(D41) R^(D10) H L_(B504) R^(D41)R^(D12) H L_(B505) R^(D41) R^(D15) H L_(B506) R^(D41) R^(D16) H L_(B507)R^(D41) R^(D17) H L_(B508) R^(D41) R^(D18) H L_(B509) R^(D41) R^(D19) HL_(B510) R^(D41) R^(D20) H L_(B511) R^(D41) R^(D21) H L_(B512) R^(D41)R^(D23) H L_(B513) R^(D41) R^(D24) H L_(B514) R^(D41) R^(D25) H L_(B515)R^(D41) R^(D27) H L_(B516) R^(D41) R^(D28) H L_(B517) R^(D41) R^(D29) HL_(B518) R^(D41) R^(D30) H L_(B519) R^(D41) R^(D31) H L_(B520) R^(D41)R^(D32) H L_(B521) R^(D41) R^(D33) H L_(B522) R^(D41) R^(D34) H L_(B523)R^(D41) R^(D42) H L_(B524) R^(D41) R^(D64) H L_(B525) R^(D41) R^(D66) HL_(B526) R^(D41) R^(D68) H L_(B527) R^(D41) R^(D76) H L_(B528) R^(D64)R^(D5) H L_(B529) R^(D64) R^(D6) H L_(B530) R^(D64) R^(D9) H L_(B531)R^(D64) R^(D10) H L_(B532) R^(D64) R^(D12) H L_(B533) R^(D64) R^(D15) HL_(B534) R^(D64) R^(D16) H L_(B535) R^(D64) R^(D17) H L_(B536) R^(D64)R^(D18) H L_(B537) R^(D64) R^(D19) H L_(B538) R^(D64) R^(D20) H L_(B539)R^(D64) R^(D21) H L_(B540) R^(D64) R^(D23) H L_(B541) R^(D64) R^(D24) HL_(B542) R^(D64) R^(D25) H L_(B543) R^(D64) R^(D27) H L_(B544) R^(D64)R^(D28) H L_(B545) R^(D64) R^(D29) H L_(B546) R^(D64) R^(D30) H L_(B547)R^(D64) R^(D31) H L_(B548) R^(D64) R^(D32) H L_(B549) R^(D64) R^(D33) HL_(B550) R^(D64) R^(D34) H L_(B551) R^(D64) R^(D42) H L_(B552) R^(D64)R^(D64) H L_(B553) R^(D64) R^(D66) H L_(B554) R^(D64) R^(D68) H L_(B555)R^(D64) R^(D76) H L_(B556) R^(D66) R^(D5) H L_(B557) R^(D66) R^(D6) HL_(B558) R^(D66) R^(D9) H L_(B559) R^(D66) R^(D10) H L_(B560) R^(D66)R^(D12) H L_(B561) R^(D66) R^(D15) H L_(B562) R^(D66) R^(D16) H L_(B563)R^(D66) R^(D17) H L_(B564) R^(D66) R^(D18) H L_(B565) R^(D66) R^(D19) HL_(B566) R^(D66) R^(D20) H L_(B567) R^(D66) R^(D21) H L_(B568) R^(D66)R^(D23) H L_(B569) R^(D66) R^(D24) H L_(B570) R^(D66) R^(D25) H L_(B571)R^(D66) R^(D27) H L_(B572) R^(D66) R^(D28) H L_(B573) R^(D66) R^(D29) HL_(B574) R^(D66) R^(D30) H L_(B575) R^(D66) R^(D31) H L_(B576) R^(D66)R^(D32) H L_(B577) R^(D66) R^(D33) H L_(B578) R^(D66) R^(D34) H L_(B579)R^(D66) R^(D42) H L_(B580) R^(D66) R^(D68) H L_(B581) R^(D66) R^(D76) HL_(B582) R^(D68) R^(D5) H L_(B583) R^(D68) R^(D6) H L_(B584) R^(D68)R^(D9) H L_(B585) R^(D68) R^(D10) H L_(B586) R^(D68) R^(D12) H L_(B587)R^(D68) R^(D15) H L_(B588) R^(D68) R^(D16) H L_(B589) R^(D68) R^(D17) HL_(B590) R^(D68) R^(D18) H L_(B591) R^(D68) R^(D19) H L_(B592) R^(D68)R^(D20) H L_(B593) R^(D68) R^(D21) H L_(B594) R^(D68) R^(D23) H L_(B595)R^(D68) R^(D24) H L_(B596) R^(D68) R^(D25) H L_(B597) R^(D68) R^(D27) HL_(B598) R^(D68) R^(D28) H L_(B599) R^(D68) R^(D29) H L_(B600) R^(D68)R^(D30) H L_(B601) R^(D68) R^(D31) H L_(B602) R^(D68) R^(D32) H L_(B603)R^(D68) R^(D33) H L_(B604) R^(D68) R^(D34) H L_(B605) R^(D68) R^(D42) HL_(B606) R^(D68) R^(D76) H L_(B607) R^(D76) R^(D5) H L_(B608) R^(D76)R^(D6) H L_(B609) R^(D76) R^(D9) H L_(B610) R^(D76) R^(D10) H L_(B611)R^(D76) R^(D12) H L_(B612) R^(D76) R^(D15) H L_(B613) R^(D76) R^(D16) HL_(B614) R^(D76) R^(D17) H L_(B615) R^(D76) R^(D18) H L_(B616) R^(D76)R^(D19) H L_(B617) R^(D76) R^(D20) H L_(B618) R^(D76) R^(D21) H L_(B619)R^(D76) R^(D23) H L_(B620) R^(D76) R^(D24) H L_(B621) R^(D76) R^(D25) HL_(B622) R^(D76) R^(D27) H L_(B623) R^(D76) R^(D28) H L_(B624) R^(D76)R^(D29) H L_(B625) R^(D76) R^(D30) H L_(B626) R^(D76) R^(D31) H L_(B627)R^(D76) R^(D32) H L_(B628) R^(D76) R^(D33) H L_(B629) R^(D76) R^(D34) HL_(B630) R^(D76) R^(D42) H L_(B631) R^(D1) R^(D1) R^(D1) L_(B632) R^(D2)R^(D2) R^(D1) L_(B633) R^(D3) R^(D3) R^(D1) L_(B634) R^(D4) R^(D4)R^(D1) L_(B635) R^(D5) R^(D5) R^(D1) L_(B636) R^(D6) R^(D6) R^(D1)L_(B637) R^(D7) R^(D7) R^(D1) L_(B638) R^(D8) R^(D8) R^(D1) L_(B639)R^(D9) R^(D9) R^(D1) L_(B640) R^(D10) R^(D10) R^(D1) L_(B641) R^(D11)R^(D11) R^(D1) L_(B642) R^(D12) R^(D12) R^(D1) L_(B643) R^(D13) R^(D13)R^(D1) L_(B644) R^(D14) R^(D14) R^(D1) L_(B645) R^(D15) R^(D15) R^(D1)L_(B646) R^(D16) R^(D16) R^(D1) L_(B647) R^(D17) R^(D17) R^(D1) L_(B648)R^(D18) R^(D18) R^(D1) L_(B649) R^(D19) R^(D19) R^(D1) L_(B650) R^(D20)R^(D20) R^(D1) L_(B651) R^(D21) R^(D21) R^(D1) L_(B652) R^(D22) R^(D22)R^(D1) L_(B653) R^(D23) R^(D23) R^(D1) L_(B654) R^(D24) R^(D24) R^(D1)L_(B655) R^(D25) R^(D25) R^(D1) L_(B656) R^(D26) R^(D26) R^(D1) L_(B657)R^(D27) R^(D27) R^(D1) L_(B658) R^(D28) R^(D28) R^(D1) L_(B659) R^(D29)R^(D29) R^(D1) L_(B660) R^(D30) R^(D30) R^(D1) L_(B661) R^(D31) R^(D31)R^(D1) L_(B662) R^(D32) R^(D32) R^(D1) L_(B663) R^(D33) R^(D33) R^(D1)L_(B664) R^(D34) R^(D34) R^(D1) L_(B665) R^(D35) R^(D35) R^(D1) L_(B666)R^(D40) R^(D40) R^(D1) L_(B667) R^(D41) R^(D41) R^(D1) L_(B668) R^(D42)R^(D42) R^(D1) L_(B669) R^(D64) R^(D64) R^(D1) L_(B670) R^(D66) R^(D66)R^(D1) L_(B671) R^(D68) R^(D68) R^(D1) L_(B672) R^(D76) R^(D76) R^(D1)L_(B673) R^(D1) R^(D2) R^(D1) L_(B674) R^(D1) R^(D3) R^(D1) L_(B675)R^(D1) R^(D4) R^(D1) L_(B676) R^(D1) R^(D5) R^(D1) L_(B677) R^(D1)R^(D6) R^(D1) L_(B678) R^(D1) R^(D7) R^(D1) L_(B679) R^(D1) R^(D8)R^(D1) L_(B680) R^(D1) R^(D9) R^(D1) L_(B681) R^(D1) R^(D10) R^(D1)L_(B682) R^(D1) R^(D11) R^(D1) L_(B683) R^(D1) R^(D12) R^(D1) L_(B684)R^(D1) R^(D13) R^(D1) L_(B685) R^(D1) R^(D14) R^(D1) L_(B686) R^(D1)R^(D15) R^(D1) L_(B687) R^(D1) R^(D16) R^(D1) L_(B688) R^(D1) R^(D17)R^(D1) L_(B689) R^(D1) R^(D18) R^(D1) L_(B690) R^(D1) R^(D19) R^(D1)L_(B691) R^(D1) R^(D20) R^(D1) L_(B692) R^(D1) R^(D21) R^(D1) L_(B693)R^(D1) R^(D22) R^(D1) L_(B694) R^(D1) R^(D23) R^(D1) L_(B695) R^(D1)R^(D24) R^(D1) L_(B696) R^(D1) R^(D25) R^(D1) L_(B697) R^(D1) R^(D26)R^(D1) L_(B698) R^(D1) R^(D27) R^(D1) L_(B699) R^(D1) R^(D28) R^(D1)L_(B700) R^(D1) R^(D29) R^(D1) L_(B701) R^(D1) R^(D30) R^(D1) L_(B702)R^(D1) R^(D31) R^(D1) L_(B703) R^(D1) R^(D32) R^(D1) L_(B704) R^(D1)R^(D33) R^(D1) L_(B705) R^(D1) R^(D34) R^(D1) L_(B706) R^(D1) R^(D35)R^(D1) L_(B707) R^(D1) R^(D40) R^(D1) L_(B708) R^(D1) R^(D41) R^(D1)L_(B709) R^(D1) R^(D42) R^(D1) L_(B710) R^(D1) R^(D64) R^(D1) L_(B711)R^(D1) R^(D66) R^(D1) L_(B712) R^(D1) R^(D68) R^(D1) L_(B713) R^(D1)R^(D76) R^(D1) L_(B714) R^(D2) R^(D1) R^(D1) L_(B715) R^(D2) R^(D3)R^(D1) L_(B716) R^(D2) R^(D4) R^(D1) L_(B717) R^(D2) R^(D5) R^(D1)L_(B718) R^(D2) R^(D6) R^(D1) L_(B719) R^(D2) R^(D7) R^(D1) L_(B720)R^(D2) R^(D8) R^(D1) L_(B721) R^(D2) R^(D9) R^(D1) L_(B722) R^(D2)R^(D10) R^(D1) L_(B723) R^(D2) R^(D11) R^(D1) L_(B724) R^(D2) R^(D12)R^(D1) L_(B725) R^(D2) R^(D13) R^(D1) L_(B726) R^(D2) R^(D14) R^(D1)L_(B727) R^(D2) R^(D15) R^(D1) L_(B728) R^(D2) R^(D16) R^(D1) L_(B729)R^(D2) R^(D17) R^(D1) L_(B730) R^(D2) R^(D18) R^(D1) L_(B731) R^(D2)R^(D19) R^(D1) L_(B732) R^(D2) R^(D20) R^(D1) L_(B733) R^(D2) R^(D21)R^(D1) L_(B734) R^(D2) R^(D22) R^(D1) L_(B735) R^(D2) R^(D23) R^(D1)L_(B736) R^(D2) R^(D24) R^(D1) L_(B737) R^(D2) R^(D25) R^(D1) L_(B738)R^(D2) R^(D26) R^(D1) L_(B739) R^(D2) R^(D27) R^(D1) L_(B740) R^(D2)R^(D28) R^(D1) L_(B741) R^(D2) R^(D29) R^(D1) L_(B742) R^(D2) R^(D30)R^(D1) L_(B743) R^(D2) R^(D31) R^(D1) L_(B744) R^(D2) R^(D32) R^(D1)L_(B745) R^(D2) R^(D33) R^(D1) L_(B746) R^(D2) R^(D34) R^(D1) L_(B747)R^(D2) R^(D35) R^(D1) L_(B748) R^(D2) R^(D40) R^(D1) L_(B749) R^(D2)R^(D41) R^(D1) L_(B750) R^(D2) R^(D42) R^(D1) L_(B751) R^(D2) R^(D64)R^(D1) L_(B752) R^(D2) R^(D66) R^(D1) L_(B753) R^(D2) R^(D68) R^(D1)L_(B754) R^(D2) R^(D76) R^(D1) L_(B755) R^(D3) R^(D4) R^(D1) L_(B756)R^(D3) R^(D5) R^(D1) L_(B757) R^(D3) R^(D6) R^(D1) L_(B758) R^(D3)R^(D7) R^(D1) L_(B759) R^(D3) R^(D8) R^(D1) L_(B760) R^(D3) R^(D9)R^(D1) L_(B761) R^(D3) R^(D10) R^(D1) L_(B762) R^(D3) R^(D11) R^(D1)L_(B763) R^(D3) R^(D12) R^(D1) L_(B764) R^(D3) R^(D13) R^(D1) L_(B765)R^(D3) R^(D14) R^(D1) L_(B766) R^(D3) R^(D15) R^(D1) L_(B767) R^(D3)R^(D16) R^(D1) L_(B768) R^(D3) R^(D17) R^(D1) L_(B769) R^(D3) R^(D18)R^(D1) L_(B770) R^(D3) R^(D19) R^(D1) L_(B771) R^(D3) R^(D20) R^(D1)L_(B772) R^(D3) R^(D21) R^(D1) L_(B773) R^(D3) R^(D22) R^(D1) L_(B774)R^(D3) R^(D23) R^(D1) L_(B775) R^(D3) R^(D24) R^(D1) L_(B776) R^(D3)R^(D25) R^(D1) L_(B777) R^(D3) R^(D26) R^(D1) L_(B778) R^(D3) R^(D27)R^(D1) L_(B779) R^(D3) R^(D28) R^(D1) L_(B780) R^(D3) R^(D29) R^(D1)L_(B781) R^(D3) R^(D30) R^(D1) L_(B782) R^(D3) R^(D31) R^(D1) L_(B783)R^(D3) R^(D32) R^(D1) L_(B784) R^(D3) R^(D33) R^(D1) L_(B785) R^(D3)R^(D34) R^(D1) L_(B786) R^(D3) R^(D35) R^(D1) L_(B787) R^(D3) R^(D40)R^(D1) L_(B788) R^(D3) R^(D41) R^(D1) L_(B789) R^(D3) R^(D42) R^(D1)L_(B790) R^(D3) R^(D64) R^(D1) L_(B791) R^(D3) R^(D66) R^(D1) L_(B792)R^(D3) R^(D68) R^(D1) L_(B793) R^(D3) R^(D76) R^(D1) L_(B794) R^(D4)R^(D5) R^(D1) L_(B795) R^(D4) R^(D6) R^(D1) L_(B796) R^(D4) R^(D7)R^(D1) L_(B797) R^(D4) R^(D8) R^(D1) L_(B798) R^(D4) R^(D9) R^(D1)L_(B799) R^(D4) R^(D10) R^(D1) L_(B800) R^(D4) R^(D11) R^(D1) L_(B801)R^(D4) R^(D12) R^(D1) L_(B802) R^(D4) R^(D13) R^(D1) L_(B803) R^(D4)R^(D14) R^(D1) L_(B804) R^(D4) R^(D15) R^(D1) L_(B805) R^(D4) R^(D16)R^(D1) L_(B806) R^(D4) R^(D17) R^(D1) L_(B807) R^(D4) R^(D18) R^(D1)L_(B808) R^(D4) R^(D19) R^(D1) L_(B809) R^(D4) R^(D20) R^(D1) L_(B810)R^(D4) R^(D21) R^(D1) L_(B811) R^(D4) R^(D22) R^(D1) L_(B812) R^(D4)R^(D23) R^(D1) L_(B813) R^(D4) R^(D24) R^(D1) L_(B814) R^(D4) R^(D25)R^(D1) L_(B815) R^(D4) R^(D26) R^(D1) L_(B816) R^(D4) R^(D27) R^(D1)L_(B817) R^(D4) R^(D28) R^(D1) L_(B818) R^(D4) R^(D29) R^(D1) L_(B819)R^(D4) R^(D30) R^(D1) L_(B820) R^(D4) R^(D31) R^(D1) L_(B821) R^(D4)R^(D32) R^(D1) L_(B822) R^(D4) R^(D33) R^(D1) L_(B823) R^(D4) R^(D34)R^(D1) L_(B824) R^(D4) R^(D35) R^(D1) L_(B825) R^(D4) R^(D40) R^(D1)L_(B826) R^(D4) R^(D41) R^(D1) L_(B827) R^(D4) R^(D42) R^(D1) L_(B828)R^(D4) R^(D64) R^(D1) L_(B829) R^(D4) R^(D66) R^(D1) L_(B830) R^(D4)R^(D68) R^(D1) L_(B831) R^(D4) R^(D76) R^(D1) L_(B832) R^(D4) R^(D1)R^(D1) L_(B833) R^(D7) R^(D5) R^(D1) L_(B834) R^(D7) R^(D6) R^(D1)L_(B835) R^(D7) R^(D8) R^(D1) L_(B836) R^(D7) R^(D9) R^(D1) L_(B837)R^(D7) R^(D10) R^(D1) L_(B838) R^(D7) R^(D11) R^(D1) L_(B839) R^(D7)R^(D12) R^(D1) L_(B840) R^(D7) R^(D13) R^(D1) L_(B841) R^(D7) R^(D14)R^(D1) L_(B842) R^(D7) R^(D15) R^(D1) L_(B843) R^(D7) R^(D16) R^(D1)L_(B844) R^(D7) R^(D17) R^(D1) L_(B845) R^(D7) R^(D18) R^(D1) L_(B846)R^(D7) R^(D19) R^(D1) L_(B847) R^(D7) R^(D20) R^(D1) L_(B848) R^(D7)R^(D21) R^(D1) L_(B849) R^(D7) R^(D22) R^(D1) L_(B850) R^(D7) R^(D23)R^(D1) L_(B851) R^(D7) R^(D24) R^(D1) L_(B852) R^(D7) R^(D25) R^(D1)L_(B853) R^(D7) R^(D26) R^(D1) L_(B854) R^(D7) R^(D27) R^(D1) L_(B855)R^(D7) R^(D28) R^(D1) L_(B856) R^(D7) R^(D29) R^(D1) L_(B857) R^(D7)R^(D30) R^(D1) L_(B858) R^(D7) R^(D31) R^(D1) L_(B859) R^(D7) R^(D32)R^(D1) L_(B860) R^(D7) R^(D33) R^(D1) L_(B861) R^(D7) R^(D34) R^(D1)L_(B862) R^(D7) R^(D35) R^(D1) L_(B863) R^(D7) R^(D40) R^(D1) L_(B864)R^(D7) R^(D41) R^(D1) L_(B865) R^(D7) R^(D42) R^(D1) L_(B866) R^(D7)R^(D64) R^(D1) L_(B867) R^(D7) R^(D66) R^(D1) L_(B868) R^(D7) R^(D68)R^(D1) L_(B869) R^(D7) R^(D76) R^(D1) L_(B870) R^(D8) R^(D5) R^(D1)L_(B871) R^(D8) R^(D6) R^(D1) L_(B872) R^(D8) R^(D9) R^(D1) L_(B873)R^(D8) R^(D10) R^(D1) L_(B874) R^(D8) R^(D11) R^(D1) L_(B875) R^(D8)R^(D12) R^(D1) L_(B876) R^(D8) R^(D13) R^(D1) L_(B877) R^(D8) R^(D14)R^(D1) L_(B878) R^(D8) R^(D15) R^(D1) L_(B879) R^(D8) R^(D16) R^(D1)L_(B880) R^(D8) R^(D17) R^(D1) L_(B881) R^(D8) R^(D18) R^(D1) L_(B882)R^(D8) R^(D19) R^(D1) L_(B883) R^(D8) R^(D20) R^(D1) L_(B884) R^(D8)R^(D21) R^(D1) L_(B885) R^(D8) R^(D22) R^(D1) L_(B886) R^(D8) R^(D23)R^(D1) L_(B887) R^(D8) R^(D24) R^(D1) L_(B888) R^(D8) R^(D25) R^(D1)L_(B889) R^(D8) R^(D26) R^(D1) L_(B890) R^(D8) R^(D27) R^(D1) L_(B891)R^(D8) R^(D28) R^(D1) L_(B892) R^(D8) R^(D29) R^(D1) L_(B893) R^(D8)R^(D30) R^(D1) L_(B894) R^(D8) R^(D31) R^(D1) L_(B895) R^(D8) R^(D32)R^(D1) L_(B896) R^(D8) R^(D33) R^(D1) L_(B897) R^(D8) R^(D34) R^(D1)L_(B898) R^(D8) R^(D35) R^(D1) L_(B899) R^(D8) R^(D40) R^(D1) L_(B900)R^(D8) R^(D41) R^(D1) L_(B901) R^(D8) R^(D42) R^(D1) L_(B902) R^(D8)R^(D64) R^(D1) L_(B903) R^(D8) R^(D66) R^(D1) L_(B904) R^(D8) R^(D68)R^(D1) L_(B905) R^(D8) R^(D76) R^(D1) L_(B906) R^(D11) R^(D5) R^(D1)L_(B907) R^(D11) R^(D6) R^(D1) L_(B908) R^(D11) R^(D9) R^(D1) L_(B909)R^(D11) R^(D10) R^(D1) L_(B910) R^(D11) R^(D12) R^(D1) L_(B911) R^(D11)R^(D13) R^(D1) L_(B912) R^(D11) R^(D14) R^(D1) L_(B913) R^(D11) R^(D15)R^(D1) L_(B914) R^(D11) R^(D16) R^(D1) L_(B915) R^(D11) R^(D17) R^(D1)L_(B916) R^(D11) R^(D18) R^(D1) L_(B917) R^(D11) R^(D19) R^(D1) L_(B918)R^(D11) R^(D20) R^(D1) L_(B919) R^(D11) R^(D21) R^(D1) L_(B920) R^(D11)R^(D22) R^(D1) L_(B921) R^(D11) R^(D23) R^(D1) L_(B922) R^(D11) R^(D24)R^(D1) L_(B923) R^(D11) R^(D25) R^(D1) L_(B924) R^(D11) R^(D26) R^(D1)L_(B925) R^(D11) R^(D27) R^(D1) L_(B926) R^(D11) R^(D28) R^(D1) L_(B927)R^(D11) R^(D29) R^(D1) L_(B928) R^(D11) R^(D30) R^(D1) L_(B929) R^(D11)R^(D31) R^(D1) L_(B930) R^(D11) R^(D32) R^(D1) L_(B931) R^(D11) R^(D33)R^(D1) L_(B932) R^(D11) R^(D34) R^(D1) L_(B933) R^(D11) R^(D35) R^(D1)L_(B934) R^(D11) R^(D40) R^(D1) L_(B935) R^(D11) R^(D41) R^(D1) L_(B936)R^(D11) R^(D42) R^(D1) L_(B937) R^(D11) R^(D64) R^(D1) L_(B938) R^(D11)R^(D66) R^(D1) L_(B939) R^(D11) R^(D68) R^(D1) L_(B940) R^(D11) R^(D76)R^(D1) L_(B941) R^(D13) R^(D5) R^(D1) L_(B942) R^(D13) R^(D6) R^(D1)L_(B943) R^(D13) R^(D9) R^(D1) L_(B944) R^(D13) R^(D10) R^(D1) L_(B945)R^(D13) R^(D12) R^(D1) L_(B946) R^(D13) R^(D14) R^(D1) L_(B947) R^(D13)R^(D15) R^(D1) L_(B948) R^(D13) R^(D16) R^(D1) L_(B949) R^(D13) R^(D17)R^(D1) L_(B950) R^(D13) R^(D18) R^(D1) L_(B951) R^(D13) R^(D19) R^(D1)L_(B952) R^(D13) R^(D20) R^(D1) L_(B953) R^(D13) R^(D21) R^(D1) L_(B954)R^(D13) R^(D22) R^(D1) L_(B955) R^(D13) R^(D23) R^(D1) L_(B956) R^(D13)R^(D24) R^(D1) L_(B957) R^(D13) R^(D25) R^(D1) L_(B958) R^(D13) R^(D26)R^(D1) L_(B959) R^(D13) R^(D27) R^(D1) L_(B960) R^(D13) R^(D28) R^(D1)L_(B961) R^(D13) R^(D29) R^(D1) L_(B962) R^(D13) R^(D30) R^(D1) L_(B963)R^(D13) R^(D31) R^(D1) L_(B964) R^(D13) R^(D32) R^(D1) L_(B965) R^(D13)R^(D33) R^(D1) L_(B966) R^(D13) R^(D34) R^(D1) L_(B967) R^(D13) R^(D35)R^(D1) L_(B968) R^(D13) R^(D40) R^(D1) L_(B969) R^(D13) R^(D41) R^(D1)L_(B970) R^(D13) R^(D42) R^(D1) L_(B971) R^(D13) R^(D64) R^(D1) L_(B972)R^(D13) R^(D66) R^(D1) L_(B973) R^(D13) R^(D68) R^(D1) L_(B974) R^(D13)R^(D76) R^(D1) L_(B975) R^(D14) R^(D5) R^(D1) L_(B976) R^(D14) R^(D6)R^(D1) L_(B977) R^(D14) R^(D9) R^(D1) L_(B978) R^(D14) R^(D10) R^(D1)L_(B979) R^(D14) R^(D12) R^(D1) L_(B980) R^(D14) R^(D15) R^(D1) L_(B981)R^(D14) R^(D16) R^(D1) L_(B982) R^(D14) R^(D17) R^(D1) L_(B983) R^(D14)R^(D18) R^(D1) L_(B984) R^(D14) R^(D19) R^(D1) L_(B985) R^(D14) R^(D20)R^(D1) L_(B986) R^(D14) R^(D21) R^(D1) L_(B987) R^(D14) R^(D22) R^(D1)L_(B988) R^(D14) R^(D23) R^(D1) L_(B989) R^(D14) R^(D24) R^(D1) L_(B990)R^(D14) R^(D25) R^(D1) L_(B991) R^(D14) R^(D26) R^(D1) L_(B992) R^(D14)R^(D27) R^(D1) L_(B993) R^(D14) R^(D28) R^(D1) L_(B994) R^(D14) R^(D29)R^(D1) L_(B995) R^(D14) R^(D30) R^(D1) L_(B996) R^(D14) R^(D31) R^(D1)L_(B997) R^(D14) R^(D32) R^(D1) L_(B998) R^(D14) R^(D33) R^(D1) L_(B999)R^(D14) R^(D34) R^(D1) L_(B1000) R^(D14) R^(D35) R^(D1) L_(B1001)R^(D14) R^(D40) R^(D1) L_(B1002) R^(D14) R^(D41) R^(D1) L_(B1003)R^(D14) R^(D42) R^(D1) L_(B1004) R^(D14) R^(D64) R^(D1) L_(B1005)R^(D14) R^(D66) R^(D1) L_(B1006) R^(D14) R^(D68) R^(D1) L_(B1007)R^(D14) R^(D76) R^(D1) L_(B1008) R^(D22) R^(D5) R^(D1) L_(B1009) R^(D22)R^(D6) R^(D1) L_(B1010) R^(D22) R^(D9) R^(D1) L_(B1011) R^(D22) R^(D10)R^(D1) L_(B1012) R^(D22) R^(D12) R^(D1) L_(B1013) R^(D22) R^(D15) R^(D1)L_(B1014) R^(D22) R^(D16) R^(D1) L_(B1015) R^(D22) R^(D17) R^(D1)L_(B1016) R^(D22) R^(D18) R^(D1) L_(B1017) R^(D22) R^(D19) R^(D1)L_(B1018) R^(D22) R^(D20) R^(D1) L_(B1019) R^(D22) R^(D21) R^(D1)L_(B1020) R^(D22) R^(D23) R^(D1) L_(B1021) R^(D22) R^(D24) R^(D1)L_(B1022) R^(D22) R^(D25) R^(D1) L_(B1023) R^(D22) R^(D26) R^(D1)L_(B1024) R^(D22) R^(D27) R^(D1) L_(B1025) R^(D22) R^(D28) R^(D1)L_(B1026) R^(D22) R^(D29) R^(D1) L_(B1027) R^(D22) R^(D30) R^(D1)L_(B1028) R^(D22) R^(D31) R^(D1) L_(B1029) R^(D22) R^(D32) R^(D1)L_(B1030) R^(D22) R^(D33) R^(D1) L_(B1031) R^(D22) R^(D34) R^(D1)L_(B1032) R^(D22) R^(D35) R^(D1) L_(B1033) R^(D22) R^(D40) R^(D1)L_(B1034) R^(D22) R^(D41) R^(D1) L_(B1035) R^(D22) R^(D42) R^(D1)L_(B1036) R^(D22) R^(D64) R^(D1) L_(B1037) R^(D22) R^(D66) R^(D1)L_(B1038) R^(D22) R^(D68) R^(D1) L_(B1039) R^(D22) R^(D76) R^(D1)L_(B1040) R^(D26) R^(D5) R^(D1) L_(B1041) R^(D26) R^(D6) R^(D1)L_(B1042) R^(D26) R^(D9) R^(D1) L_(B1043) R^(D26) R^(D10) R^(D1)L_(B1044) R^(D26) R^(D12) R^(D1) L_(B1045) R^(D26) R^(D15) R^(D1)L_(B1046) R^(D26) R^(D16) R^(D1) L_(B1047) R^(D26) R^(D17) R^(D1)L_(B1048) R^(D26) R^(D18) R^(D1) L_(B1049) R^(D26) R^(D19) R^(D1)L_(B1050) R^(D26) R^(D20) R^(D1) L_(B1051) R^(D26) R^(D21) R^(D1)L_(B1052) R^(D26) R^(D23) R^(D1) L_(B1053) R^(D26) R^(D24) R^(D1)L_(B1054) R^(D26) R^(D25) R^(D1) L_(B1055) R^(D26) R^(D27) R^(D1)L_(B1056) R^(D26) R^(D28) R^(D1) L_(B1057) R^(D26) R^(D29) R^(D1)L_(B1058) R^(D26) R^(D30) R^(D1) L_(B1059) R^(D26) R^(D31) R^(D1)L_(B1060) R^(D26) R^(D32) R^(D1) L_(B1061) R^(D26) R^(D33) R^(D1)L_(B1062) R^(D26) R^(D34) R^(D1) L_(B1063) R^(D26) R^(D35) R^(D1)L_(B1064) R^(D26) R^(D40) R^(D1) L_(B1065) R^(D26) R^(D41) R^(D1)L_(B1066) R^(D26) R^(D42) R^(D1) L_(B1067) R^(D26) R^(D64) R^(D1)L_(B1068) R^(D26) R^(D66) R^(D1) L_(B1069) R^(D26) R^(D68) R^(D1)L_(B1070) R^(D26) R^(D76) R^(D1) L_(B1071) R^(D35) R^(D5) R^(D1)L_(B1072) R^(D35) R^(D6) R^(D1) L_(B1073) R^(D35) R^(D9) R^(D1)L_(B1074) R^(D35) R^(D10) R^(D1) L_(B1075) R^(D35) R^(D12) R^(D1)L_(B1076) R^(D35) R^(D15) R^(D1) L_(B1077) R^(D35) R^(D16) R^(D1)L_(B1078) R^(D35) R^(D17) R^(D1) L_(B1079) R^(D35) R^(D18) R^(D1)L_(B1080) R^(D35) R^(D19) R^(D1) L_(B1081) R^(D35) R^(D20) R^(D1)L_(B1082) R^(D35) R^(D21) R^(D1) L_(B1083) R^(D35) R^(D23) R^(D1)L_(B1084) R^(D35) R^(D24) R^(D1) L_(B1085) R^(D35) R^(D25) R^(D1)L_(B1086) R^(D35) R^(D27) R^(D1) L_(B1087) R^(D35) R^(D28) R^(D1)L_(B1088) R^(D35) R^(D29) R^(D1) L_(B1089) R^(D35) R^(D30) R^(D1)L_(B1090) R^(D35) R^(D31) R^(D1) L_(B1091) R^(D35) R^(D32) R^(D1)L_(B1092) R^(D35) R^(D33) R^(D1) L_(B1093) R^(D35) R^(D34) R^(D1)L_(B1094) R^(D35) R^(D40) R^(D1) L_(B1095) R^(D35) R^(D41) R^(D1)L_(B1096) R^(D35) R^(D42) R^(D1) L_(B1097) R^(D35) R^(D64) R^(D1)L_(B1098) R^(D35) R^(D66) R^(D1) L_(B1099) R^(D35) R^(D68) R^(D1)L_(B1100) R^(D35) R^(D76) R^(D1) L_(B1101) R^(D40) R^(D5) R^(D1)L_(B1102) R^(D40) R^(D6) R^(D1) L_(B1103) R^(D40) R^(D9) R^(D1)L_(B1104) R^(D40) R^(D10) R^(D1) L_(B1105) R^(D40) R^(D12) R^(D1)L_(B1106) R^(D40) R^(D15) R^(D1) L_(B1107) R^(D40) R^(D16) R^(D1)L_(B1108) R^(D40) R^(D17) R^(D1) L_(B1109) R^(D40) R^(D18) R^(D1)L_(B1110) R^(D40) R^(D19) R^(D1) L_(B1111) R^(D40) R^(D20) R^(D1)L_(B1112) R^(D40) R^(D21) R^(D1) L_(B1113) R^(D40) R^(D23) R^(D1)L_(B1114) R^(D40) R^(D24) R^(D1) L_(B1115) R^(D40) R^(D25) R^(D1)L_(B1116) R^(D40) R^(D27) R^(D1) L_(B1117) R^(D40) R^(D28) R^(D1)L_(B1118) R^(D40) R^(D29) R^(D1) L_(B1119) R^(D40) R^(D30) R^(D1)L_(B1120) R^(D40) R^(D31) R^(D1) L_(B1121) R^(D40) R^(D32) R^(D1)L_(B1122) R^(D40) R^(D33) R^(D1) L_(B1123) R^(D40) R^(D34) R^(D1)L_(B1124) R^(D40) R^(D41) R^(D1) L_(B1125) R^(D40) R^(D42) R^(D1)L_(B1126) R^(D40) R^(D64) R^(D1) L_(B1127) R^(D40) R^(D66) R^(D1)L_(B1128) R^(D40) R^(D68) R^(D1) L_(B1129) R^(D40) R^(D76) R^(D1)L_(B1130) R^(D41) R^(D5) R^(D1) L_(B1131) R^(D41) R^(D6) R^(D1)L_(B1132) R^(D41) R^(D9) R^(D1) L_(B1133) R^(D41) R^(D10) R^(D1)L_(B1134) R^(D41) R^(D12) R^(D1) L_(B1135) R^(D41) R^(D15) R^(D1)L_(B1136) R^(D41) R^(D16) R^(D1) L_(B1137) R^(D41) R^(D17) R^(D1)L_(B1138) R^(D41) R^(D18) R^(D1) L_(B1139) R^(D41) R^(D19) R^(D1)L_(B1140) R^(D41) R^(D20) R^(D1) L_(B1141) R^(D41) R^(D21) R^(D1)L_(B1142) R^(D41) R^(D23) R^(D1) L_(B1143) R^(D41) R^(D24) R^(D1)L_(B1144) R^(D41) R^(D25) R^(D1) L_(B1145) R^(D41) R^(D27) R^(D1)L_(B1146) R^(D41) R^(D28) R^(D1) L_(B1147) R^(D41) R^(D29) R^(D1)L_(B1148) R^(D41) R^(D30) R^(D1) L_(B1149) R^(D41) R^(D31) R^(D1)L_(B1150) R^(D41) R^(D32) R^(D1) L_(B1151) R^(D41) R^(D33) R^(D1)L_(B1152) R^(D41) R^(D34) R^(D1) L_(B1153) R^(D41) R^(D42) R^(D1)L_(B1154) R^(D41) R^(D64) R^(D1) L_(B1155) R^(D41) R^(D66) R^(D1)L_(B1156) R^(D41) R^(D68) R^(D1) L_(B1157) R^(D41) R^(D76) R^(D1)L_(B1158) R^(D64) R^(D5) R^(D1) L_(B1159) R^(D64) R^(D6) R^(D1)L_(B1160) R^(D64) R^(D9) R^(D1) L_(B1161) R^(D64) R^(D10) R^(D1)L_(B1162) R^(D64) R^(D12) R^(D1) L_(B1163) R^(D64) R^(D15) R^(D1)L_(B1164) R^(D64) R^(D16) R^(D1) L_(B1165) R^(D64) R^(D17) R^(D1)L_(B1166) R^(D64) R^(D18) R^(D1) L_(B1167) R^(D64) R^(D19) R^(D1)L_(B1168) R^(D64) R^(D20) R^(D1) L_(B1169) R^(D64) R^(D21) R^(D1)L_(B1170) R^(D64) R^(D23) R^(D1) L_(B1171) R^(D64) R^(D24) R^(D1)L_(B1172) R^(D64) R^(D25) R^(D1) L_(B1173) R^(D64) R^(D27) R^(D1)L_(B1174) R^(D64) R^(D28) R^(D1) L_(B1175) R^(D64) R^(D29) R^(D1)L_(B1176) R^(D64) R^(D30) R^(D1) L_(B1177) R^(D64) R^(D31) R^(D1)L_(B1178) R^(D64) R^(D32) R^(D1) L_(B1179) R^(D64) R^(D33) R^(D1)L_(B1180) R^(D64) R^(D34) R^(D1) L_(B1181) R^(D64) R^(D42) R^(D1)L_(B1182) R^(D64) R^(D64) R^(D1) L_(B1183) R^(D64) R^(D66) R^(D1)L_(B1184) R^(D64) R^(D68) R^(D1) L_(B1185) R^(D64) R^(D76) R^(D1)L_(B1186) R^(D66) R^(D5) R^(D1) L_(B1187) R^(D66) R^(D6) R^(D1)L_(B1188) R^(D66) R^(D9) R^(D1) L_(B1189) R^(D66) R^(D10) R^(D1)L_(B1190) R^(D66) R^(D12) R^(D1) L_(B1191) R^(D66) R^(D15) R^(D1)L_(B1192) R^(D66) R^(D16) R^(D1) L_(B1193) R^(D66) R^(D17) R^(D1)L_(B1194) R^(D66) R^(D18) R^(D1) L_(B1195) R^(D66) R^(D19) R^(D1)L_(B1196) R^(D66) R^(D20) R^(D1) L_(B1197) R^(D66) R^(D21) R^(D1)L_(B1198) R^(D66) R^(D23) R^(D1) L_(B1199) R^(D66) R^(D24) R^(D1)L_(B1200) R^(D66) R^(D25) R^(D1) L_(B1201) R^(D66) R^(D27) R^(D1)L_(B1202) R^(D66) R^(D28) R^(D1) L_(B1203) R^(D66) R^(D29) R^(D1)L_(B1204) R^(D66) R^(D30) R^(D1) L_(B1205) R^(D66) R^(D31) R^(D1)L_(B1206) R^(D66) R^(D32) R^(D1) L_(B1207) R^(D66) R^(D33) R^(D1)L_(B1208) R^(D66) R^(D34) R^(D1) L_(B1209) R^(D66) R^(D42) R^(D1)L_(B1210) R^(D66) R^(D68) R^(D1) L_(B1211) R^(D66) R^(D76) R^(D1)L_(B1212) R^(D68) R^(D5) R^(D1) L_(B1213) R^(D68) R^(D6) R^(D1)L_(B1214) R^(D68) R^(D9) R^(D1) L_(B1215) R^(D68) R^(D10) R^(D1)L_(B1216) R^(D68) R^(D12) R^(D1) L_(B1217) R^(D68) R^(D15) R^(D1)L_(B1218) R^(D68) R^(D16) R^(D1) L_(B1219) R^(D68) R^(D17) R^(D1)L_(B1220) R^(D68) R^(D18) R^(D1) L_(B1221) R^(D68) R^(D19) R^(D1)L_(B1222) R^(D68) R^(D20) R^(D1) L_(B1223) R^(D68) R^(D21) R^(D1)L_(B1224) R^(D68) R^(D23) R^(D1) L_(B1225) R^(D68) R^(D24) R^(D1)L_(B1226) R^(D68) R^(D25) R^(D1) L_(B1227) R^(D68) R^(D27) R^(D1)L_(B1228) R^(D68) R^(D28) R^(D1) L_(B1229) R^(D68) R^(D29) R^(D1)L_(B1230) R^(D68) R^(D30) R^(D1) L_(B1231) R^(D68) R^(D31) R^(D1)L_(B1232) R^(D68) R^(D32) R^(D1) L_(B1233) R^(D68) R^(D33) R^(D1)L_(B1234) R^(D68) R^(D34) R^(D1) L_(B1235) R^(D68) R^(D42) R^(D1)L_(B1236) R^(D68) R^(D76) R^(D1) L_(B1237) R^(D76) R^(D5) R^(D1)L_(B1238) R^(D76) R^(D6) R^(D1) L_(B1239) R^(D76) R^(D9) R^(D1)L_(B1240) R^(D76) R^(D10) R^(D1) L_(B1241) R^(D76) R^(D12) R^(D1)L_(B1242) R^(D76) R^(D15) R^(D1) L_(B1243) R^(D76) R^(D16) R^(D1)L_(B1244) R^(D76) R^(D17) R^(D1) L_(B1245) R^(D76) R^(D18) R^(D1)L_(B1246) R^(D76) R^(D19) R^(D1) L_(B1247) R^(D76) R^(D20) R^(D1)L_(B1248) R^(D76) R^(D21) R^(D1) L_(B1249) R^(D76) R^(D23) R^(D1)L_(B1250) R^(D76) R^(D24) R^(D1) L_(B1251) R^(D76) R^(D25) R^(D1)L_(B1252) R^(D76) R^(D27) R^(D1) L_(B1253) R^(D76) R^(D28) R^(D1)L_(B1254) R^(D76) R^(D29) R^(D1) L_(B1255) R^(D76) R^(D30) R^(D1)L_(B1256) R^(D76) R^(D31) R^(D1) L_(B1257) R^(D76) R^(D32) R^(D1)L_(B1258) R^(D76) R^(D33) R^(D1) L_(B1259) R^(D76) R^(D34) R^(D1)L_(B1260) R^(D76) R^(D42) R^(D1)

wherein R^(D1) to R^(D81) has the following structures:


12. A formulation comprising the compound of claim
 1. 13. A chemicalstructure selected from the group consisting of a monomer, a polymer, amacromolecule, and a supramolecule, wherein the chemical structurecomprises the compound according to claim
 1. 14. The compound of claim1, wherein the L_(A) is selected from the group


15. The compound of claim 1, wherein the compound is selected from thegroup consisting of:


16. An organic light emitting device (OLED) comprising: an anode; acathode; and an organic layer, disposed between the anode and thecathode, comprising a compound comprising a ligand L_(A) of Formula I:

wherein Ring B represents a five- or six-membered aromatic ring; whereinR³ represents from none to the maximum number of substitutions; whereinX¹, X², X³, and X⁴ are each independently a CR or N; wherein at leasttwo adjacent ones of X¹, X², X³, and X⁴ are CR and fused into afive-membered aromatic ring; wherein R¹ is CR¹¹R¹²R¹³ or join with R² toform into a ring; wherein R, R¹, R², R³, R¹¹, R¹², and R¹³ are eachindependently selected from the group consisting of hydrogen, deuterium,halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy,amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl,heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile,sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;wherein any two substituents among R, R¹, R², and R³ are optionallyjoined to form into an aromatic ring; wherein two substituents amongR¹¹, R¹², and R¹³ are optionally joined to form into a ring; whereinL_(A) is coordinated to a metal M; wherein L_(A) is optionally linkedwith other ligands to comprise a tridentate, tetradentate, pentadentate,or hexadentate ligand; and wherein M is optionally coordinated to otherligands.
 17. The OLED of claim 16, wherein the organic layer is anemissive layer and the compound is an emissive dopant or a non-emissivedopant.
 18. The OLED of claim 16, wherein the organic layer furthercomprises a host, wherein host comprises at least one chemical groupselected from the group consisting of carbazole, dibenzothiophene,dibenzofuran, dibenzoselenophene, azacarbazole, aza-dibenzothiophene,aza-dibenzofuran, and aza-dibenzoselenophene.
 19. The OLED of claim 16,wherein the organic layer further comprises a host, wherein the host isselected from the group consisting of:

and combinations thereof.
 20. A consumer product comprising an organiclight emitting device comprising: an anode; a cathode; and an organiclayer, disposed between the anode and the cathode, comprising a compoundcomprising a ligand L_(A) of Formula I:

wherein Ring B represents a five- or six-membered aromatic ring; whereinR³ represents from none to the maximum number of substitutions; whereinX¹, X², X³, and X⁴ are each independently a CR or N; wherein at leasttwo adjacent ones of X¹, X², X³, and X⁴ are CR and fused into afive-membered aromatic ring; wherein R¹ is CR¹¹R¹²R¹³ or join with R² toform into a ring; wherein R, R¹, R², R³, R¹¹, R¹², and R¹³ are eachindependently selected from the group consisting of hydrogen, deuterium,halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy,amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl,heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile,sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;wherein any two substituents among R, R¹, R², and R³ are optionallyjoined to form into an aromatic ring; wherein two substituents amongR¹¹, R¹², and R¹³ are optionally joined to form into a ring; whereinL_(A) is coordinated to a metal M; wherein L_(A) is optionally linkedwith other ligands to comprise a tridentate, tetradentate, pentadentate,or hexadentate ligand; and wherein M is optionally coordinated to otherligands.